Rna array compositions and methods

ABSTRACT

Described herein are RNA arrays, and compositions and methods for generating RNA arrays, particularly high density RNA arrays. The disclosed methods for generating RNA arrays utilize template DNA arrays and RNA polymerase to generate RNA arrays. In some embodiments, the disclosed methods use an RNA polymerase and modified ribonucleosides to generate modified RNA arrays for various applications, e.g. RNA arrays having higher nuclease resistance, more conformationally stable RNA arrays, and higher binding affinity RNA aptamer arrays. In some embodiments, the disclosed methods are used to generate RNA bead arrays.

CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application claims priority to U.S. Provisional Patent Application Ser. No. 61/723,011, filed on Nov. 6, 2012, which is incorporated by reference herein in its entirety.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with government support under DK093467 and HG004952 awarded by the National Institutes of Health. The government has certain rights in the invention.

BACKGROUND

High density DNA microarrays have been commercially available worldwide for more than a decade, but high density RNA microarrays do not exist yet due to the difficulty of equivalent high density RNA synthesis methods. The development of RNA arrays, and especially high density RNA arrays would enable a number important new applications including, for example, fabrication of RNA aptamer arrays; identification of RNA sequences that produce fluorescence from non-fluorescent small molecules; identification and characterization of novel ribozymes and RNA-binding proteins. Thus, there is an ongoing need for high density RNA arrays and methods for generating them.

BRIEF SUMMARY

Described herein are RNA and template array compositions and methods for generating such compositions. The methods and compositions are based on the finding that DNA arrays can serve as a template for RNA-polymerase-based synthesis of complementary RNA arrays.

Accordingly, in one aspect described herein is an RNA array comprising RNAs that are covalently linked at their 5′ ends to a solid support.

In some embodiments, the covalently linked RNAs represent at least 10 unique RNA sequences and have a feature density of at least 20 features/cm².

In some embodiments the RNAs comprise at least about 20 unique RNA sequences. In other embodiments the RNAs represent at least about 50 unique RNA sequences.

In some embodiments the length of the at least ten unique RNA sequences is about 20 bases to about 50 bases. In some embodiments the density of single-stranded RNAs in the RNA array is about 200 features/cm².

In some embodiments the RNAs in the RNA array comprise modified ribonucleotides. In one embodiment the modified ribonucleotides are RNase resistant (e.g., 2′-fluoro ribonucleotides or 2′-methoxyribonucleotides).

In another aspect provided herein is a template array comprising: (i) an array of single-stranded template DNA oligonucleotides linked at their 3′ ends to a solid support, comprising a consensus sequence, and capped by a protecting group at their 5′ ends; and (ii) single-stranded RNA primers that are covalently linked at their 5′ ends to the solid support, and that are complementary to the consensus sequence, wherein the single-stranded RNA primers hybridize to the single-stranded template DNA oligonucleotides.

In some embodiments the single-stranded RNA primers have a length of about 4 bases to about 20 bases. In one embodiment, the single-stranded RNA primers have a length of about 13 bases.

In some embodiments the single-stranded template DNA oligonucleotides or single-stranded RNA primers are covalently linked to the solid support through a polyethylene glycol spacer.

In some embodiments the protecting group to be added to the 5′ end of the single-stranded template DNA oligonucleotides is an acetyl group or a phenoxyacetyl group.

In some embodiments a kit is provided that includes the above-mentioned template array and any of (i) an RNA polymerase; (ii) ribonucleoside triphosphates; and (iii) a DNase. In some embodiments the ribonucleoside triphosphates to be included in the kit are modified ribonucleoside triphosphates. In some embodiments, the included modified ribonucleoside triphosphates are modified ribonucleosides (e.g., 2′-fluoro ribonucleosides, 2′-methoxy ribonucleosides, 2′-amino ribonucleosides, 5-bromouridine-5′-triphosphate, 4-thiouridine-5′-triphosphate, 6-thioguanosine-5′-triphosphate).

In a further aspect disclosed herein is a method for generating a template array, which includes the steps of: (i) providing a solid support comprising a layer of protected deoxyribonucleosides that comprise a 5′-photolabile protecting group and are covalently linked at their 3′ end to a spacer layer bound to the solid support; (ii) irradiating the layer of protected deoxyribonucleosides with ultraviolet energy sufficient to deprotect about half of the protected deoxyribonucleosides; (iii) coupling the deprotected deoxyribonucleosides with a ribonucleoside phosphoramidite comprising a 5′ acid-labile protecting group; (iv) irradiating the remaining protected deoxyribonucleosides with ultraviolet irradiation sufficient to deprotect all of the remaining protected deoxyribonucleoside phosphoramidites; (v) extending the deprotected deoxyribonucleosides, at one or more locations, by light-directed 3′ to 5′ photolithographic synthesis to generate template DNA oligonucleotides;

(vi) coupling a protecting group to the 5′ ends of the template DNA oligonucleotides;

(vii) removing the 5′ acid-labile protecting groups on the protected ribonucleosides by acid treatment; and

(viii) extending the deprotected ribonucleosides, at one or more locations, by 5′ to 3′ chemical synthesis of RNA primers comprising a sequence that is complementary to a sequence at the 3′ end of the template DNA strands to obtain a template array.

In some embodiments of the above-mentioned method, the 5′ acid-labile protecting group in step (iii) includes a 4,4′-dimethoxytrityl (DMT) group.

In some embodiments the protecting group coupled to the 5′-ends of the template DNA strands in step (vi) is a phenoxyacetyl group or an acetyl group.

In some embodiments RNase-resistant modified ribonucleoside phosphoramidites are used in the extension of the deprotected ribonucleosides to obtain RNase-resistant RNA primers in step (viii). In some embodiments, where RNase-resistant modified ribonucleoside phosphoramidites are used, the RNase-resistant modified ribonucleoside phosphoramidites are 2′-fluoro ribonucleoside phosphoramidites or 2′-methoxy ribonucleoside phosphoramidites.

In a further aspect described herein is a method for generating an RNA array, comprising the steps of (i) providing a template array of (a) single-stranded template DNAs linked at their 3′ ends to a solid support and comprising a consensus sequence; and (b) single-stranded RNA primers that are covalently linked at their 5′ ends to the solid support, and that are complementary to the consensus sequence of the single-stranded template DNAs; (ii) hybridizing the single-stranded RNA primers with the single-stranded template DNAs; (iii) extending the hybridized RNA primers along the single-stranded template DNAs using an RNA polymerase and ribonucleoside triphosphates to obtain double-stranded DNA-RNA hybrids; and (iv) exposing the DNA-RNA hybrids to a DNase enzyme to remove the template DNAs from the DNA-RNA hybrids to obtain an RNA array.

In some embodiments the RNA polymerase in step (iii) is T7 RNA polymerase or T3 RNA polymerase.

In some embodiments the ribonucleoside triphosphates used in step (iii) are modified ribonucleoside triphosphates. In one embodiment, the modified ribonucleoside triphosphates are RNase-resistant modified ribonucleoside triphosphates. In some embodiments the RNase-resistant modified ribonucleoside triphosphates to be used are 2′-fluoro ribonucleoside triphosphates or 2′-methoxy ribonucleoside triphosphates.

In some embodiments the method can also include a step of synthesizing the single-stranded RNA primers in the array prior to step (i).

In some embodiments the single-stranded template DNAs represent at least 20 unique sequences. In other embodiments the single-stranded template DNAs represent at least 50 unique sequences.

In yet another aspect provided herein is a method to generate an RNA bead pool, comprising: (i) providing beads comprising 5′-linked RNA primers comprising a consensus sequence; (ii) hybridizing the 5′-linked RNA primers with DNA oligonucleotides comprising a unique template sequence and a sequence complementary to the consensus sequence, wherein the DNA oligonucleotides are provided in solution; (iii) extending the hybridized RNA primers along the single-stranded template DNAs using an RNA polymerase and ribonucleoside triphosphates to obtain double-stranded DNA-RNA hybrids; and contacting the DNA-RNA hybrids with a DNase to remove the template DNAs from the DNA-RNA hybrids to obtain an RNA bead pool.

INCORPORATION BY REFERENCE

All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, and patent application was specifically and individually indicated to be incorporated by reference.

BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee. The present invention will be better understood and features, aspects and advantages other than those set forth above will become apparent when consideration is given to the following detailed description thereof. Such detailed description makes reference to the following drawings, wherein:

FIG. 1 shows a schematic overview of an exemplary embodiment of an RNA array synthesis method starting from a solid support coated with a PEG 2000 spacer layer linked to photolabile NPPOC-protected, deoxyribonucleosides at their 3′ end. UV light irradiation is controlled so as to deprotect about half of the 3′-linked deoxyribonucleosides. The deprotected deoxyribonucleosides are then coupled to an acid-labile DMT-protected ribonucleoside phosphoramidite. UV light irradiation is then used to deprotect the remaining NPPOC-protected deoxyribonucleosides. Following this deprotection step, photolithographic 3′ to 5′ synthesis is used to generate an array of template DNA oligonucleotides, comprising an initial consensus sequence of approximately 12 bases that is common to most or all positions and a downstream sequence that is unique for each position or subsets of positions in the array. After template DNA oligonucleotide synthesis is completed, the DNA oligonucleotides are capped by acetylation at their 5′ ends. The DMT-protected ribonucleoside phosphoramidites are then deprotected by acid treatment. Chemical synthesis, with 2-methoxy ribonucleoside phosphoramidites, is then used to generate a 5′-linked RNA primer comprising a sequence that is complementary to the template DNA consensus sequence mentioned above. Hybridization of the synthesized RNA primers with the consensus sequence in the template DNA oligonucleotides is then used to generate a cRNA copy of each unique template DNA oligonucleotide sequence using T7 RNA polymerase or in some cases, T3 RNA polymerase, in the presence of ribonucleoside triphosphates, or in some cases, RNase-resistant ribonucleoside triphosphates. After RNA polymerase synthesis of RNAs is complete, template DNA is eliminated from the array by digestion with DNase leaving behind an RNA array ready for use.

FIG. 2 (A) shows a schematic illustration of how 5′-fluorescent labeled IGFBP1 DNA probe amplicons are generated to test an RNA array. After generation of IGFBP1 amplicons, these double-stranded products were partially digested with T7 exonuclease to yield double-stranded products with single-stranded overhangs capable of hybridizing with RNAs present in the RNA array. As shown, the ability of the fluorescently labeled, exonuclease-digested probe to hybridize with RNAs on the array depends on the amount of sequence overlap between the single-stranded probe overhang and the RNA in question. (B) Shows an RNA array fluorescent hybridization signal consistent with the 5′ to 3′ tiled pattern of the RNAs in the array, where stronger hybridization signal indicates more complementary overlap with the single-stranded overhang in the DNA probe, and less or no signal where less or no overlap occurred.

FIG. 3. Top panels are images of fluorescent DNA probes hybridized to an RNA array enzymatically synthesized using unmodified ribonucleosides (top left panel), and the same type of RNA array after RNase A treatment (top right panel), which resulted in complete degradation of the RNA array as indicated by the total loss of hybridization signal. In the bottom panels are images of 2′-fluoro RNA arrays that were enzymatically synthesized using a 2′-fluorine-modified nucleoside triphosphate mix (left bottom panel) and the same type of RNA array and 2′-fluoro RNA array after RNase A treatment (bottom right panel), which shows only a partial loss of hybridization signal indicating that 2′-fluoro RNA arrays are relatively resistant to RNase.

FIG. 4 shows a fluorescence image of a patterned array of DNAs, RNAs, and modified RNAs after various treatment conditions and hybridization to complementary probe sequences labeled with distinct fluorophores. The dimensions of the “Badger Chemist” array are about 6 mm×5 mm, which consists of the “body”, the “sweater/flask” and the “lab coat” sequences (Table 3). The natural RNA and 2′-fluoro RNA array were treated with DNase I and RNase A, sequentially, while the DNA array was treated with RNase A and then DNase I. The arrays were visualized by hybridization with their DNA complements labeled with FAM (sweater/flask), Texas Red (body), and Cy5 (lab coat).

FIG. 5 shows a fluorescence image of a patterned array of DNAs, RNAs, and modified RNAs before and after DNase treatment, and followed by hybridization to complementary probe sequences labeled with distinct fluorophores. (A) The schematic diagram of 10-23 DNAZyme cleavage test on RNA array. B) The dimensions of “Badger Chemist” array are about 6 mm×5 mm, which consists of the “body,” the “sweater/flask” and the “lab coat” sequences (Table 3). The arrays were visualized by hybridization with the three corresponding oligodeoxynucleotide complements, tagged respectively with the fluorophores fluorescein (sweater/flask), Texas Red (body), and Cy 5 (lab coat). The “lab coat” sequences were intact on the DNA array, whereas 70% were cleaved on the natural RNA array and 55% were cleaved on the 2′-fluoro RNA array. It is noted there were fewer cleavage events on the 2′-fluoro RNA array than on the natural RNA array. Although the purine nucleobases, which participated in cleavage events, were not 2′-fluoro modified, we speculate the halogenated groups in the ribose rings of pyrimidine nucleobases would interfere with RNA:DNA duplex formation and result in different efficiency. This is the first report showing the different cleavage activities of 10-23 DNAzyme on natural RNA and 2′-fluoro RNA molecules.

FIG. 6 shows a fluorescence image of a 24-2-min RNA aptamer array. The array was incubated with the chromophore 3,5-difluoro-4-hydroxybenzylidene imidazolinone (DFHBI) (24-2), which fluoresces upon binding to the RNA aptamer sequence. After incubation with DFHBI, the array was visualized using a GeneTac UC 4×4 microarray scanner with a 488 nm blue excitation laser and a 512 nm emission filter.

DETAILED DESCRIPTION

Described herein are RNA array compositions and methods for generating such compositions. The methods and compositions are based on the finding that DNA arrays, e.g., high density DNA arrays can serve as templates for RNA-polymerase-based synthesis of a complementary RNA array. Many possible applications for RNA arrays can be envisioned, including, but not limited to, deciphering the binding specificities of RNA-binding proteins, as a tool to aid in the engineering of sequence-specific RNA-binding proteins, for screening and characterizing RNA-based therapeutics, for fabricating tiling arrays of RNA viral genomes, for fabricating miRNA arrays, engineering ribozyme arrays, discovering new ribozymes, studying ribozyme function, engineering artificial siRNAs and miRNAs, fabricating mRNA tiling arrays, and searching for miRNA “sponges” (molecules that bind to and inactivate miRNAs).

It is to be understood that this invention is not limited to the particular methodology, protocols, materials, and reagents described, as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims.

It must be noted that as used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural reference unless the context clearly dictates otherwise. As well, the terms “a” (or “an”), “one or more” and “at least one” can be used interchangeably herein. It is also to be noted that the terms “comprising”, “including”, and “having” can be used interchangeably.

Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications and patents specifically mentioned herein are incorporated by reference for all purposes including describing and disclosing the chemicals, cell lines, vectors, animals, instruments, statistical analysis and methodologies which are reported in the publications which might be used in connection with the invention. All references cited in this specification are to be taken as indicative of the level of skill in the art. Nothing herein is to be construed as an admission that the invention is not entitled to antedate such disclosure by virtue of prior invention.

The practice of the present invention will employ, unless otherwise indicated, conventional techniques of medicinal chemistry, pharmacology, organic chemistry, analytical chemistry, molecular biology, microbiology, and immunology, which are within the skill of the art. Such techniques are explained fully in the literature.

I. DEFINITIONS

In describing the embodiments and claiming the invention, the following terminology will be used in accordance with the definitions set out below.

As used herein, “about” means within 5% of a stated range within the relevant parameter.

As used herein, “RNase-resistant” refers to a modified RNA having reduction in susceptibility to RNase degradation or the ability of a modified ribonucleoside to confer a reduction in susceptibility of an RNA to RNase degradation by at least 10%.

II. Methods

Disclosed herein are methods for generating a template array and for generating RNA arrays using such template arrays.

In an exemplary embodiment, generating a template array starts from a solid support material such as amorphous carbon, glassy carbon, polymer or silanized glass that is coated with a layer of spacer material (e.g., PEG 2000 or PEG 4500) covalently linked to deoxyribonucleoside phosphoramidites (“bridging moieties”) protected by a photolabile protecting group, e.g., 3′-nitrophenylpropyloxycarbonyl (NPPOC). In other embodiments, the solid support material is provided in the form of silica beads in the size range of 1 to 10 microns. The NPPOC-protected spacer layer is then irradiated with a suitable amount of deprotecting dose of UV light (e.g., 0.5 joule on amorphous carbon on gold, 0.75 joule on glassy carbon at about 365 nm in the working examples provided herein) to remove about half of the NPPOC protecting groups on the spacer layer, which deprotects hydroxyl groups on half of the deoxyribonucleosides covalently linked to the spacer layer. The deoxyribonucleosides with deprotected, free hydroxyl groups are then coupled with an acid-labile protecting group such as 4,4′-dimethoxytrityl (DMT)-protected ribonucleoside phosphoramidites. Afterwards, a full dose of UV light is used to remove all of the remaining photolabile protecting groups from the spacer layer, which allows the light-directed 3′ to 5′ photolithographic synthesis of DNA arrays starting from the newly deprotected deoxyribonucleoside phosphoramidites. Methods for 3′ to 5′ photolithographic synthesis of DNA oligonucleotide arrays are known in the art, as described in, e.g., Wu et at (2012), Angewandte Chimie Int Ed Engl 51(19):4628-4632. The initial 8 to about 15 deoxynucleotides (e.g., 9, 10, 11, 12, 13, or 14 deoxynucleotides) attained by photolithographic DNA synthesis encompass a “consensus” sequence that is common to the single-stranded template DNAs to be synthesized. For example, in one embodiment, the consensus sequence is 3′-CCTGTGCCGCTT-5 (SEQ ID NO:1). After 3′ to 5′ photolithographic synthesis of the consensus sequence, a variety of positionally-determined template sequences are synthesized in a desired pattern in the length range of about 20 deoxyribonucleotides to about 80 deoxyribonucleotides. After photolithographic synthesis of the template DNA strands, these are protected “capped” by a phenoxyacetyl group or an acetyl group at the 5′ end to block undesired further synthesis. Finally, the acid-labile DMT protecting groups on the 5′-linked, protected ribonucleoside phosphoramidites are removed by acid treatment (e.g., with 2% trichloroacetic acid or 3% dichloroacetic acid in dichloromethane) to expose 3′ hydroxyl groups of the 5′-linked ribonucleosides for chemical synthesis of an RNA primer complementary consensus sequence. The template array can be used to generate an RNA array, as described below.

In some embodiments, the spacer layer, deoxyribonucleoside or ribonucleoside is protected with an acid-labile protecting group, such as 4,4′-DMT rather than a photolabile protecting group. In this case, partial deprotection of the layer is achieved by treatment with a dilute solution of dichloro- or trichloroacetic acid, reduced exposure time to the acid, or both (e.g., with 2% trichloroacetic acid or 3% dichloroacetic acid in dichloromethane for 50 seconds or more). The deoxyribonucleosides with deprotected, free hydroxyl groups are then coupled with a photolabile protecting group such as NPPOC. Afterwards, a higher concentration of the deprotecting acid is used to remove all of the remaining acid-labile protecting groups from the spacer layer, which allows the light-directed 3′ to 5′ photolithographic synthesis of DNA arrays starting from the newly deprotected deoxyribonucleoside phosphoramidites. After photolithographic synthesis of the template DNA strands, these are protected “capped” by a phenoxyacetyl group or an acetyl group at the 5′ end to block undesired further synthesis. Finally, the photolabile NPPOC protecting groups on the 5′-linked, protected ribonucleoside phosphoramidites are removed by irradiation with UV light to expose 3′ hydroxyl groups of the 5′-linked ribonucleosides for chemical synthesis of an RNA primer complementary consensus sequence.

In some embodiments the length of the template DNA strands ranges from about 20 bases to about 80 bases, e.g., about 25 bases, 27 bases, 28 bases, 29 bases, 35 bases, 40 bases, 60 bases, 70 bases, or another length from about 20 bases to about 80 bases.

In some embodiments the template DNA strands to be synthesized can be synthesized to obtain a range of template DNA strand densities ranging from about 20 to about 1,000,000 features/cm², e.g., about 25, 30, 40, 50, 60, 65, 70, 75, 80, 100, 120, 150, 200, 300, 500, 750, 1,000, 2,000, 2,500, 3,000, 3,500, 3,750, 4,200, 4,500, 5,000, 6,000, 6,500, 7,000, 7,500, 8,000, 9,000, 20,000, 50,000, 100,000, 200,000, 400,000, 500,000, 600,000, 700,000, 800,000, 900,000, or another feature density from about 20 features/cm² to about 1,000,000 features/cm².

In various embodiments the template DNA strands to be synthesized represent at least 20 unique sequences to about 1,000,000 unique sequences, e.g., 30, 50, 100, 130, 145, 148, 150, 155, 160, 200, 500, 1,000, 1,500, 2,000, 3,000, 5,000, 10,000, 15,000, 20,000, 50,000, 100,000, 200,000, 400,000, 500,000, 600,000, 700,000, 800,000, 900,000, or another number of unique sequences. In some embodiments the template DNA oligonucleotide sequences comprise a series of subsequences that are shifted relative to each other by a single terminal nucleotide, where the template DNA oligonucleotide sequences, in aggregate, cover a longer contiguous sequence, e.g., a genomic DNA sequence, a cDNA sequence, a vector sequence etc. In one embodiment, the template DNA oligonucleotides are synthesized in a tiling pattern that covers a source sequence, e.g., a genomic promoter sequence, in order in the 5′ to 3′ direction.

In various embodiments the RNA primer sequences generated in the template array are approximately the same size as the template consensus sequence in the range of about 4 ribonucleotides to about 20 ribonucleotides, e.g., about 5 ribonucleotides, 6 ribonucleotides, 7 ribonucleotides, 8 ribonucleotides, 9 ribonucleotides, 10 ribonucleotides, 11 ribonucleotides, 12 ribonucleotides, 13 ribonucleotides, 14 ribonucleotides, 16 ribonucleotides, 18 ribonucleotides, 18 ribonucleotides, or another length from about 4 ribonucleotides to about 20 ribonucleotides. In an exemplary embodiment, the RNA primer sequence comprises the complementary consensus sequence: 5′-GGACACGGCGAA-3′ (SEQ ID NO:2).

In some embodiments the ribonucleoside phosphoramidites used to extend the 5′-linked ribonucleosides are RNase-resistant modified ribonucleosides. Examples of RNase-resistant modified ribonucleosides include, but are not limited to, 2-fluoro ribonucleosides, 2-amino ribonucleosides and 2-methoxy ribonucleosides.

Also described herein are methods to generate RNA arrays (including high density RNA arrays) from the above-described template arrays.

In some embodiments a method to generate an RNA array starts from a template array, which comprises an array of: (a) single-stranded template DNAs linked at their 3′ ends to a solid support and comprising a consensus sequence; and (b) single-stranded RNA primers that are covalently linked at their 5′ ends to the solid support, and that are complementary to the consensus sequence of the single-stranded template DNAs. The template RNA array is then incubated under hybridization conditions permissive for the 5′-covalently linked single-stranded RNA primers to hybridize with the complementary consensus sequence of the 3′-covalently linked single-stranded template DNAs. Suitable hybridization conditions are well known in the art, as described in, e.g., Tsai et al (2005), Molecular Biotechnology, 29(3):221-224. The hybridized RNA primers are then extended 5′ to 3′ along the single-stranded template DNAs using an RNA polymerase and ribonucleoside triphosphates to obtain double-stranded DNA-RNA hybrids. Afterwards, DNase treatment is used to eliminate template oligonucleotides within the DNA-RNA hybrids and unhybridized template DNA oligonucleotides, thereby yielding an RNA array.

In some embodiments, RNA primers, having a consensus sequence, are synthesized on a spacer layer first, to obtain a layer of 5′-linked RNA primers bound to a solid support surface. Afterwards, template DNA oligonucleotides comprising a consensus sequence at the 3′ end, and a unique sequence at a 5′ position relative to the consensus sequence, are added, in solution, to the 5′-linked RNA primer layer and hybridized. The hybridized RNA primers are then extended by an RNA polymerase to generate cRNA copies of the template DNA oligonucleotides. The DNA oligonucleotides are then removed by DNase digestion to obtain a cRNA array. In such embodiments, the unique cRNA sequence at each position is then “decoded” by sequential hybridization decoding as described in, e.g., Gunderson et al (2004), Genome Research, 14:870-877.

In some embodiments, RNA primers are 5′-linked primers on the surface of beads and comprising a consensus sequence. For individual pools of RNA-primer bound beads, a pool of template DNA oligonucleotides comprising a sequence complementary to the consensus sequence in the bead-bound primers and a unique sequence are then hybridized with the bead-bound RNA primers. Afterwards, an RNA polymerase is used to extend the hybridized bead-bound RNA primers to make bead-bound cRNAs of the template DNA oligonucleotides. The DNA is then removed to obtain a pool of bead-bound cRNAs (an “RNA bead pool”). One of ordinary skill in the art will appreciate that by using any of a number of known coding schemes (e.g., color-based or size based), RNA bead pools can be combined to obtain an RNA bead array, where each RNA bead pool within the array represents a unique RNA sequence.

In some embodiments the RNA polymerase used to extend the RNA primer is a T7 RNA polymerase or a T3 RNA polymerase. In one embodiment, the RNA polymerase to be used is T7 RNA polymerase. In some embodiments the ribonucleoside triphosphates to be used are modified ribonucleoside triphosphates. In one embodiment, the modified ribonucleoside triphosphates to be used in the method are RNase-resistant modified ribonucleoside triphosphates. Examples of suitable RNase-resistant modified ribonucleoside triphosphates include, but are not limited to, 2′-fluoro ribonucleosides and 2′-methoxy ribonucleosides. In some embodiments the modified ribonucleoside triphosphates are fluorescent modified ribonucleoside triphosphates. In cases where modified ribonucleosides are used for synthesis of array RNAs, modified ribonucleotides can be substituted for 1, 2, 3, or all four of the possible ribonucleoside types (A, U, G, C). In some embodiments for a given type of ribonucleoside, both modified and unmodified ribonucleosides are used for RNA synthesis with an RNA polymerase. The proportion of modified ribonucleotide used during RNA-polymerase-mediated RNA synthesis can range from 0 to 100%, e.g., from 5%, 10%, 20%, 30%, 50%, 60%, 70%, 90%, or another proportion of ribonucleosides to be used for RNA synthesis with an RNA polymerase.

III. COMPOSITIONS

Described herein are RNA arrays (including high density RNA arrays) and array templates.

RNA Arrays

In some embodiments the RNA arrays described herein comprise RNAs linked at their 5′ ends to a solid support. In some embodiments, the RNAs included in the high density array represent at least 20 unique RNA sequences and have a density of at least about 20 features/cm².

In some embodiments the RNAs are covalently linked at their 5′ ends to the solid support, indirectly, through a bridging moiety and a spacer covalently bound to the surface of the solid support. For example, the spacer can be a polyethylene glycol with a molecular weight of about 2000 daltons (PEG 2000) or 4500 daltons (PEG 4500). The bridging moiety, in some embodiments is a photolabile or acid-labile protected deoxynucleoside phosphoramidite covalently linked to a 3′ hydroxyl group of the spacer.

In some embodiments the 5′ ends of the RNAs in the high density RNA array encompass a sequence of about 8 to about 15 ribonucleotides (e.g., 9, 10, 12, 14 or another number of ribonucleotides from about 8 to about 15 ribonucleotides), which are termed an “RNA primer complementary consensus sequence,” herein. Typically, the RNA primer complementary consensus sequence comprises one or more 2′-methoxy ribonucleoside triphosphates, which are introduced during photolithographic synthesis of the RNA primer consensus sequence. While not wishing to be bound by theory, it is believed that the incorporation of 2-methoxyribonucleoside triphosphates facilitates hybridization by the RNA primer consensus sequence to its complement during synthesis of the high density RNA array, as described herein, and also confers RNase resistance.

In some embodiments the RNAs covalently linked to the solid support, comprise one or more modified ribonucleotides. In some embodiments the modified ribonucleotides confer resistance to ribonuclease. Examples of modified ribonucleotides that confer resistance to ribonucleases include, but are not limited to, 2′-methoxy ribonucleoside triphosphates, 2′-fluoro ribonucleoside triphosphates, 2′-amino ribonucleosides, 5-bromouridine-5′-triphosphates, 4-thiouridine-5′-triphosphates and 6-thioguanosine-5′-triphosphates. In other embodiments modified nucleotides include fluorescently modified ribonucleoside triphosphates (e.g., Cy5-ribonucleoside triphosphates) or hapten-modified ribonucleoside triphosphates (e.g., biotin-, or aminoallyl-modified ribonucleoside triphosphates) as known and used in the art. In some embodiments 100% of the constituent ribonucleotides in the RNAs of the high density RNA arrays are modified ribonucleotides. In other embodiments the proportion of modified ribonucleotides in the RNAs ranges from about 5% to about 95% of the ribonucleotides in the array RNAs, e.g., about 7%, 10%, 15%, 20%, 25%, 30%, 40%, 50%, 60%, 75%, or another proportion of the modified ribonucleotides ranging from about 5% to about 95% of the ribonucleotides. Where modified ribonucleotides are included in the array RNAs, 1, 2, 3, or all 4 of the ribonucleotides (i.e., A, U, G, or C) may include modified ribonucleotides.

Typically, the RNA arrays disclosed herein will represent at least 20 unique RNA sequences to about 1,000,000 unique RNA sequences, e.g., 30, 50, 100, 130, 145, 148, 150, 155, 160, 200, 500, 1,000, 1,500, 2,000, 3,000, 5,000, 10,000, 15,000, 20,000, 50,000, 100,000, 200,000, 400,000, 500,000, 600,000, 700,000, 800,000, 900,000, or another number of unique RNA sequences from at least 20 unique RNA sequences to about 1,000,000 unique RNA sequences. In one embodiment, the number of unique RNA sequences is about 50 to about 1,000 unique RNA sequences. In another embodiment, the number of unique RNA sequences is about 10 to about 200 unique RNA sequences. In another embodiment, the number of unique RNA sequences is about 100,000 sequences.

In various embodiments the length of the RNAs included in the disclosed RNA arrays ranges from at least about 20 ribonucleotides to about 80 ribonucleotides, e.g., about 25 ribonucleotides, 27 ribonucleotides, 28 ribonucleotides, 29 ribonucleotides, 35 ribonucleotides, 40 ribonucleotides, 60 ribonucleotides, 70 ribonucleotides, or another length from about 20 ribonucleotides to about 80 ribonucleotides.

In some embodiments the RNA arrays provided herein comprise a feature density of about 20 features/cm² to about 1,000,000 features/cm², e.g., about 25, 30, 40, 50, 60, 65, 70, 75, 80, 100, 120, 150, 200, 300, 500, 750, 1,000, 2,000, 2,500, 3,000, 3,500, 3,750, 4,200, 4,500, 5,000, 6,000, 6,500, 7,000, 7,500, 8,000, 9,000, 20,000, 50,000, 100,000, 200,000, 400,000, 500,000, 600,000, 700,000, 800,000, 900,000, or another feature density from about 20 features/cm² to about 1,000,000 features/cm². In some embodiments the disclosed RNA arrays have a feature density of about 50,000 features/cm² to about 1,000,000 features/cm².

Suitable solid support materials for RNA arrays include, but are not limited to, amorphous carbon, glassy carbon, and polymer or silanized glass. In some embodiments the solid support material used for RNA arrays is amorphous carbon.

Template Arrays

Also disclosed herein are template arrays that are useful intermediate compositions for generating the RNA arrays described herein. In some embodiments a template array comprises an array of (i) single-stranded template oligonucleotides linked at their 3′ end to a solid support, comprising a consensus sequence, and capped by a protecting group (e.g., an phenoxyacetyl group) group at their 5′ end; and (ii) single-stranded RNA primers that are covalently linked at their 5′ end to the solid support, and that are complementary to the consensus sequence, wherein the single-stranded RNA primers hybridize to the single-stranded template DNAs.

In some embodiments of the template array, the 5′ ends of the RNAs in the template array encompass a sequence of about 4 to about 20 ribonucleotides (e.g., 5, 6, 8, 9, 10, 12, 14, 16, 17, 18, or another number of ribonucleotides from about 4 to about 20 ribonucleotides), which are termed an “RNA primer complementary consensus sequence,” herein. Typically, the RNA primer complementary consensus sequence comprises one or more modified ribonucleotides (e.g., RNase-resistant ribonucleotides such as 2′-methoxy ribonucleotides or 2′-fluoro ribonucleotides), or mixtures of unmodified and modified ribonucleotides, which are introduced during synthesis of the RNA primer consensus sequence.

In various embodiments single-stranded template DNA oligonucleotides and single-stranded RNA primers are linked at their 3′ and 5′ ends, respectively, to a bridging moiety (e.g., a deoxynucleotide), which in turn is linked to a spacer such as PEG 2000 or PEG 4500. The spacer provides a means of linking the single-stranded template DNA oligonucleotides and RNA primers to a solid support for the template array. Suitable solid support materials for template arrays include any materials compatible with RNA arrays, as described herein.

In some embodiments the template arrays provided herein comprise a feature density of about 20 features/cm² to about 1,000,000 features cm², e.g., about 25, 30, 40, 50, 60, 65, 70, 75, 80, 100, 120, 150, 200, 300, 500, 750, 1,000, 2,000, 2,500, 3,000, 3,500, 3,750, 4,200, 4,500, 5,000, 6,000, 6,500, 7,000, 7,500, 8,000, 9,000, 20,000, 50,000, 100,000, 200,000, 400,000, 500,000, 600,000, 700,000, 800,000, 900,000, or another feature density from about 20 features/cm² to about 1,000,000 features/cm². In some embodiments the disclosed RNA arrays have a feature density of about 5,000 features/cm² to about 1,000,000 features/cm².

In various embodiments template DNAs and RNA primers in the above-mentioned are in situ synthesized, in a base-by-base manner, using maskless array synthesizer (MAS) technology, as described in, e.g., Phillips et al (2008), Nucleic Acids Res, 36(1).

Kits

Also disclosed herein are kits that include a template array as described herein and any of (i) an RNA polymerase; (ii) ribonucleoside triphosphates; and (iii) a DNase. For example, in some cases the kit contains a template array and ribonucleoside triphosphates. In some embodiments the ribonucleoside triphosphates included in the kit are modified ribonucleoside triphosphates that are RNase-resistant. Such modified RNase-resistant nucleotides include, but are not limited, to 2′-methoxy ribonucleoside triphosphates, 2′-fluororibonucleoside triphosphates, 2′-amino ribonucleosides, 5-bromouridine-5′-triphosphates, 4-thiouridine-5′-triphosphates, and 6-thioguanosine-5′-triphosphates. In other embodiments the template array kit includes a template array and an RNA polymerase suitable for catalyzing primer-dependent biosynthesis of RNA using a DNA template. Examples of suitable RNA polymerases include, but are not limited to T7 RNA polymerase and T3 RNA polymerase. In some embodiments the template array kit contains a template array and a DNase, e.g., DNase I, T7 exonuclease, or Rec J exonuclease.

In one embodiment, the kits disclosed herein comprise a template array, an RNA polymerase, ribonucleoside triphosphates, and a DNase.

Optionally, any of the above-mentioned kits will also include instructions for generating an RNA array from the included template array using an RNA polymerase, ribonucleoside triphosphates, and a DNase according to the methods disclosed herein.

EXAMPLES Example 1 Generation of an RNA Array from a Mouse Insulin-Like Growth Factor Binding Protein-1 (IGFPBP1) Promoter DNA Template

In contrast to high density DNA microarrays that have been commercially available worldwide for more than a decade, a high density RNA microarray has not been generated until now due to the difficulty of synthesis. Hundred bases-long DNA microarrays have been made, owing to the mature state of the art for DNA synthesis and phosphoramidite chemistry, with high fidelity having been reported. We describe here an enzymatic method to fabricate high density RNA arrays by taking advantage of the high quality and length of DNA arrays.

FIG. 1A depicts the process of fabricating a high density DNA template array to be employed for enzymatic synthesis of a high density RNA array. In an exemplary procedure, light-directed photolithographic synthesis of DNA arrays is performed on a carbon surface that is functionalized with hydroxyl groups. A quarter of the full deprotecting dose of UV light (365 nm) is used to remove half of the photolabile protecting groups (3′-nitrophenylpropyloxycarbonyl, NPPOC) on the first layer of deoxyribonucleosides, which is covalently coupled to polyethylene glycol 2000 spacers on the carbon surface. The deoxyribonucleosides with free hydroxyl groups are then coupled with acid-labile DMT (4,4′-dimethoxytrityl) protected ribonucleoside phosphoramidites. A full dose of UV light is used to remove all of the photolabile protecting groups on the first layer and enables the light-directed photolithographic synthesis of DNA arrays using the method described in Wu et al supra. The 5′ ends of DNA oligonucleotides on the surface are then capped by acetylation to block undesired synthesis from the termini. Each element of the DNA arrays includes a consensus DNA sequence at the 3′ end, which later serves as a complement to the 2′-methoxy RNA primer. Finally, the acid-labile DMT protecting groups on the first layer are removed with dichloroacetic acid to reveal 3′ hydroxyl groups of the ribonucleosides for the chemical synthesis of 2′-methoxy RNA primer, that includes the consensus sequence, in the 5′ to 3′ direction, which is then extended enzymatically by T7 RNA polymerase in a subsequent step.

FIG. 1B lays out the process of enzymatic synthesis of a high density RNA array. The oligonucleotide array was denatured and reannealed for RNA extension by T7 or T3 RNA polymerase). Either unmodified or fluorinated ribonucleoside triphosphates can be used for the synthesis of unmodified or 2′-fluorine-modified RNA oligonucleotides for better resistance to RNase. DNA endonuclease, e.g., DNase I, is then used to remove the DNA template from the array to yield the final high density RNA array.

To demonstrate proof of concept, an RNA tiling array was fabricated to characterize the products of a T7 exonuclease (a 5′ dsDNA exonuclease) digestion reaction. The RNA tiling array allowed us to optimize the generation of single-stranded DNA for sequence-specific capture on the RNA array. We fabricated an RNA tiling array containing all possible 20mer complements, thereby spanning the entire 180 base long IGFBP1 promoter DNA in 161 single-base increments (see Text 1 for the target sequence, Table 1 for design of the “DNA template array”, and Table 2 for the copied “tiling RNA array”).

The DNA fragment corresponding to positions −205 to −25 of the mouse IGFBP1 promoter was amplified by PCR from NIH 3T3 (mouse embryonic fibroblast cell line) genomic DNA (purchased from New England Biolabs, MA, USA):

The primer sequences used to amplify the IGFBP1 promoter amplicon are: 5′-TTA GCT CCT GTC CCA GTC CAT-3′ (SEQ ID NO:4) and 5′-TAT GAA GGG CTG GCT GTG C-3′ (SEQ ID NO:5). A 5′ phosphorothioate protected oligonucleotide with 6-carboxyfluorescein (FAM) tag (5′-T*/iFluorT/A GCT CCT GTC CCA GTC CAT-3′) (SEQ ID NO:6) was used to produce a 180 bp fluorescently tagged IGFBP1 promoter DNA amplicon

A DNA template array was generated by first synthesizing a template consensus sequence (5′-TTCGCCGTGTCC-3′) (SEQ ID NO:1) in array format. The template consensus sequence, which is complementary to an RNA primer consensus sequence, was synthesized from 3′ to 5′ at all positions on the array prior to the synthesis of the sequences in Table 1 at various positions from 3′ to 5′ using 5′-NPPOC-protected deoxyribonucleoside phosphoramidites. Afterwards, the position-specific sequences were also synthesized 3′ to 5′. So, for example, at locations in the array, where the sequence position is listed as “1-20” in Table 1, the actual complete sequence at those locations on the array, is ‘: 3′-CCTGTGCCGCTT-ACCTGACCCTGTCCTCGATT-5′ (SEQ ID NO:7) (where the underlining indicates the complement of the RNA consensus sequence).

The sequences listed in Table 1 served as the DNA templates for an RNA polymerase extension reaction to produce the RNA array that could be used to capture IGFBP1 promoter DNA.

DNA quality control probe 1 (DNA QC1) is the complementary sequence to the fluorescently labeled ssDNA called “ApoE” for quality control purposes. DNA quality probe 2 (DNA QC2) is the complementary sequence to the fluorescently labeled ssDNA called “w1282” for quality control purposes. DNA quality probe 3 (DNA QC3) is the same probe sequence as the fluorescently labeled ssDNA called “ApoE” for quality control purposes. DNA quality probe 4 (DNA QC4) is the same probe sequence as the fluorescently labeled ssDNA called “w1282” for quality control purposes.

The fluorescently labeled “ApoE” ssDNA is capturable to QC1 but not QC3 in the template array. The fluorescently labeled “w1282” ssDNA is capturable to QC2 but not QC4 in the “template DNA array.

TABLE 1 IGFBP1 promoter template DNA array oligonucleotide sequences. Name/Position DNA Sequence (3′->5′) Blank DNA QC1 CGGCTACTGGACGTTCTCA (SEQ ID NO: 8) DNA QC2 TATTGAAACGTTGTCACC (SEQ ID NO: 9) DNA QC3 TGAGAACGTCCAGTAGCCG (SEQ ID NO: 10) DNA QC4 GGTGACAACGTTTCAATA (SEQ ID NO: 11) 161 to 180 3′-ATACTTCCCGACCGACACGC-5′ (SEQ ID NO: 12) 160 to 179 TACTTCCCGACCGACACGCC (SEQ ID NO: 13) 159 to 178 ACTTCCCGACCGACACGCCG (SEQ ID NO: 14) 158 to 177 CTTCCCGACCGACACGCCGT (SEQ ID NO: 15) 157 to 176 TTCCCGACCGACACGCCGTG (SEQ ID NO: 16) 156 to 175 TCCCGACCGACACGCCGTGT (SEQ ID NO: 17) 155 to 174 CCCGACCGACACGCCGTGTC (SEQ ID NO: 18) 154 to 173 CCGACCGACACGCCGTGTCC (SEQ ID NO: 19) 153 to 172 CGACCGACACGCCGTGTCCA (SEQ ID NO: 20) 152 to 171 GACCGACACGCCGTGTCCAA (SEQ ID NO: 21) 151 to 170 ACCGACACGCCGTGTCCAAT (SEQ ID NO: 22) 150 to 169 CCGACACGCCGTGTCCAATT (SEQ ID NO: 23) 149 to 168 CGACACGCCGTGTCCAATTA (SEQ ID NO: 24) 148 to 167 GACACGCCGTGTCCAATTAC (SEQ ID NO: 25) 147 to 166 ACACGCCGTGTCCAATTACT (SEQ ID NO: 26) 146 to 165 CACGCCGTGTCCAATTACTA (SEQ ID NO: 27) 145 to 164 ACGCCGTGTCCAATTACTAA (SEQ ID NO: 28) 144 to 163 CGCCGTGTCCAATTACTAAC (SEQ ID NO: 29) 143 to 162 GCCGTGTCCAATTACTAACA (SEQ ID NO: 30) 142 to 161 CCGTGTCCAATTACTAACAG (SEQ ID NO: 31) 141 to 160 CGTGTCCAATTACTAACAGT (SEQ ID NO: 32) 140 to 159 GTGTCCAATTACTAACAGTC (SEQ ID NO: 33) 139 to 158 TGTCCAATTACTAACAGTCC (SEQ ID NO: 34) 138 to 157 GTCCAATTACTAACAGTCCC (SEQ ID NO: 35) 137 to 156 TCCAATTACTAACAGTCCCG (SEQ ID NO: 36) 136 to 155 CCAATTACTAACAGTCCCGT (SEQ ID NO: 37) 135 to 154 CAATTACTAACAGTCCCGTC (SEQ ID NO: 38) 134 to 153 AATTACTAACAGTCCCGTCG (SEQ ID NO: 39) 133 to 152 ATTACTAACAGTCCCGTCGC (SEQ ID NO: 40) 132 to 151 TTACTAACAGTCCCGTCGCA (SEQ ID NO: 41) 131 to 150 TACTAACAGTCCCGTCGCAC (SEQ ID NO: 42) 130 to 149 ACTAACAGTCCCGTCGCACG (SEQ ID NO: 43) 129 to 148 CTAACAGTCCCGTCGCACGA (SEQ ID NO: 44) 128 to 147 TAACAGTCCCGTCGCACGAT (SEQ ID NO: 45) 127 to 146 AACAGTCCCGTCGCACGATC (SEQ ID NO: 46) 126 to 145 ACAGTCCCGTCGCACGATCC (SEQ ID NO: 47) 125 to 144 CAGTCCCGTCGCACGATCCT (SEQ ID NO: 48) 124 to 143 AGTCCCGTCGCACGATCCTG (SEQ ID NO: 49) 123 to 142 GTCCCGTCGCACGATCCTGG (SEQ ID NO: 50) 122 to 141 TCCCGTCGCACGATCCTGGG (SEQ ID NO: 51) 121 to 140 CCCGTCGCACGATCCTGGGG (SEQ ID NO: 52) 120 to 139 CCGTCGCACGATCCTGGGGT (SEQ ID NO: 53) 119 to 138 CGTCGCACGATCCTGGGGTC (SEQ ID NO: 54) 118 to 137 GTCGCACGATCCTGGGGTCA (SEQ ID NO: 55) 117 to 136 TCGCACGATCCTGGGGTCAC (SEQ ID NO: 56) 116 to 135 CGCACGATCCTGGGGTCACA (SEQ ID NO: 57) 115 to 134 GCACGATCCTGGGGTCACAA (SEQ ID NO: 58) 114 to 133 CACGATCCTGGGGTCACAAG (SEQ ID NO: 59) 113 to 132 ACGATCCTGGGGTCACAAGT (SEQ ID NO: 60) 112 to 131 CGATCCTGGGGTCACAAGTT (SEQ ID NO: 61) 111 to 130 GATCCTGGGGTCACAAGTTT (SEQ ID NO: 62) 110 to 129 ATCCTGGGGTCACAAGTTTT (SEQ ID NO: 63) 109 to 128 TCCTGGGGTCACAAGTTTTA (SEQ ID NO: 64) 108 to 127 CCTGGGGTCACAAGTTTTAT (SEQ ID NO: 65) 107 to 126 CTGGGGTCACAAGTTTTATT (SEQ ID NO: 66) 106 to 125 TGGGGTCACAAGTTTTATTC (SEQ ID NO: 67) 105 to1 24 GGGGTCACAAGTTTTATTCA (SEQ ID NO: 68) 104 to 123 GGGTCACAAGTTTTATTCAA (SEQ ID NO: 69) 103 to 122 GGTCACAAGTTTTATTCAAA (SEQ ID NO: 70) 102 to 121 GTCACAAGTTTTATTCAAAC (SEQ ID NO: 71) 101 to 120 TCACAAGTTTTATTCAAACA (SEQ ID NO: 72) 100 to 119 CACAAGTTTTATTCAAACAA (SEQ ID NO: 73)  99 to 118 ACAAGTTTTATTCAAACAAA (SEQ ID NO: 74)  98 to 117 CAAGTTTTATTCAAACAAAA (SEQ ID NO: 75)  97 to 116 AAGTTTTATTCAAACAAAAC (SEQ ID NO: 76)  96 to 115 AGTTTTATTCAAACAAAACG (SEQ ID NO: 77)  95 to 114 GTTTTATTCAAACAAAACGA (SEQ ID NO: 78)  94 to 113 TTTTATTCAAACAAAACGAA (SEQ ID NO: 79)  93 to 112 TTTATTCAAACAAAACGAAC (SEQ ID NO: 80)  92 to 111 TTATTCAAACAAAACGAACA (SEQ ID NO: 81)  91 to 110 TATTCAAACAAAACGAACAC (SEQ ID NO: 82)  90 to 109 ATTCAAACAAAACGAACACT (SEQ ID NO: 83)  89 to 108 TTCAAACAAAACGAACACTC (SEQ ID NO: 84)  88 to 107 TCAAACAAAACGAACACTCG (SEQ ID NO: 85)  87 to 106 CAAACAAAACGAACACTCGA (SEQ ID NO: 86)  86 to 105 AAACAAAACGAACACTCGAG (SEQ ID NO: 87)  85 to 104 AACAAAACGAACACTCGAGA (SEQ ID NO: 88)  84 to 103 ACAAAACGAACACTCGAGAT (SEQ ID NO: 89) Sequence (3′-->5′)  83 to 102 CAAAACGAAC ACTCGAGATG (SEQ ID NO: 90)  82 to 101 AAAACGAACA CTCGAGATGT (SEQ ID NO: 91)  81 to 100 AAACGAACAC TCGAGATGTG (SEQ ID NO: 92)  80 to 99 AACGAACACT CGAGATGTGT (SEQ ID NO: 93)  79 to 98 ACGAACACTC GAGATGTGTT (SEQ ID NO: 94)  78 to 97 CGAACACTCG AGATGTGTTT (SEQ ID NO: 95)  77 to 96 GAACACTCGA GATGTGTTTG (SEQ ID NO: 96)  76 to 95 AACACTCGAG ATGTGTTTGG (SEQ ID NO: 97)  75 to 94 ACACTCGAGA TGTGTTTGGC (SEQ ID NO: 98)  74 to 93 CACTCGAGAT GTGTTTGGCA (SEQ ID NO: 99)  73 to 92 ACTCGAGATG TGTTTGGCAC (SEQ ID NO: 100)  72 to 91 CTCGAGATGT GTTTGGCACC (SEQ ID NO: 101)  71 to 90 TCGAGATGTG TTTGGCACCC (SEQ ID NO: 102)  70 to 89 CGAGATGTGT TTGGCACCCA (SEQ ID NO: 103)  69 to 88 GAGATGTGTTT GGCACCCAC (SEQ ID NO: 104)  68 to 87 AGATGTGTTTG GCACCCACC (SEQ ID NO: 105)  67 to 86 GATGTGTTTGG CACCCACCT (SEQ ID NO: 106)  66 to 85 ATGTGTTTGGC ACCCACCTT (SEQ ID NO: 107)  65 to 84 TGTGTTTGGCA CCCACCTTC (SEQ ID NO: 108)  64 to 83 GTGTTTGGCAC CCACCTTCC (SEQ ID NO: 109)  63 to 82 TGTTTGGCACC CACCTTCCC (SEQ ID NO: 110)  62 to 81 GTTTGGCACCC ACCTTCCCC (SEQ ID NO: 111)  61 to 80 TTTGGCACCCA CCTTCCCCC (SEQ ID NO: 112)  60 to 79 TTGGCACCCA CCTTCCCCCA (SEQ ID NO: 113)  59 to 78 TGGCACCCAC CTTCCCCCAT (SEQ ID NO: 114)  58 to 77 GGCACCCACC TTCCCCCATT (SEQ ID NO: 115)  57 to 76 GCACCCACCTT CCCCCATTT (SEQ ID NO: 116)  56 to 75 CACCCACCTTC CCCCATTTC (SEQ ID NO: 117)  55 to 74 ACCCACCTTCC CCCATTTCC (SEQ ID NO: 118)  54 to 73 CCCACCTTCCC CCATTTCCC (SEQ ID NO: 119)  53 to 72 CCACCTTCCCC CATTTCCCT (SEQ ID NO: 120)  52 to 71 CACCTTCCCCC ATTTCCCTA (SEQ ID NO: 121)  51 to 70 ACCTTCCCCCA TTTCCCTAG (SEQ ID NO: 122)  50 to 69 CCTTCCCCCAT TTCCCTAGT (SEQ ID NO: 123)  49 to 68 CTTCCCCCATT TCCCTAGTC  48 to 67 TTCCCCCATTT CCCTAGTCC (SEQ ID NO: 124)  47 to 66 TCCCCCATTTC CCTAGTCCA (SEQ ID NO: 125)  46 to 65 CCCCCATTTCC CTAGTCCAA (SEQ ID NO: 126)  45 to 64 CCCCATTTCCC TAGTCCAAA (SEQ ID NO: 127)  44 to 63 CCCATTTCCCT AGTCCAAAA (SEQ ID NO: 128)  43 to 62 CCATTTCCCTA GTCCAAAAG  42 to 61 CATTTCCCTAG TCCAAAAGA (SEQ ID NO: 129)  41 to 60 ATTTCCCTAGT CCAAAAGAT (SEQ ID NO: 130)  40 to 59 TTTCCCTAGTC CAAAAGATG  39 to 58 TTCCCTAGTCC AAAAGATGA (SEQ ID NO: 131)  38 to 57 TCCCTAGTCCA AAAGATGAT (SEQ ID NO: 132)  37 to 56 CCCTAGTCCA AAAGATGATA (SEQ ID NO: 133)  36 to 55 CCTAGTCCAA AAGATGATAC (SEQ ID NO: 134)  35 to 54 CTAGTCCAAA AGATGATACA  34 to 53 TAGTCCAAAA GATGATACAA (SEQ ID NO: 135)  33 to 52 AGTCCAAAAG ATGATACAAA (SEQ ID NO: 136)  32 to 51 GTCCAAAAGA TGATACAAAC (SEQ ID NO: 137)  31 to 50 TCCAAAAGAT GATACAAACA (SEQ ID NO: 138)  30 to 49 CCAAAAGATG ATACAAACAG (SEQ ID NO: 139)  29 to 48 CAAAAGATGA TACAAACAGG (SEQ ID NO: 140)  28 to 47 AAAAGATGAT ACAAACAGGG (SEQ ID NO: 141)  27 to 46 AAAGATGATA CAAACAGGGC (SEQ ID NO: 142)  26 to 45 AAGATGATAC AAACAGGGCA (SEQ ID NO: 143)  25 to 44 AGATGATACA AACAGGGCAC (SEQ ID NO: 144)  24 to 43 GATGATACAA ACAGGGCACC (SEQ ID NO: 145)  23 to 42 ATGATACAAA CAGGGCACCA (SEQ ID NO: 146)  22 to 41 TGATACAAAC AGGGCACCAC (SEQ ID NO: 147)  21 to 40 GATACAAACA GGGCACCACT (SEQ ID NO: 148)  20 to 39 ATACAAACAG GGCACCACTA (SEQ ID NO: 149)  19 to 38 TACAAACAGG GCACCACTAC (SEQ ID NO: 150)  18 to 37 ACAAACAGGG CACCACTACC (SEQ ID NO: 151)  17 to 36 CAAACAGGGC ACCACTACCT (SEQ ID NO: 152)  16 to 35 AAACAGGGCA CCACTACCTG (SEQ ID NO: 153)  15 to 34 AACAGGGCAC CACTACCTGA (SEQ ID NO: 154)  14 to 33 ACAGGGCACC ACTACCTGAC (SEQ ID NO: 155)  13 to 32 CAGGGCACCA CTACCTGACC (SEQ ID NO: 156)  12 to 31 AGGGCACCAC TACCTGACCC (SEQ ID NO: 157)  11 to 30 GGGCACCACT ACCTGACCCT (SEQ ID NO: 158)  10 to 29 GGCACCACTA CCTGACCCTG (SEQ ID NO: 159)   9 to 28 GCACCACTAC CTGACCCTGT (SEQ ID NO: 160)   8 to 27 CACCACTACCT GACCCTGTC (SEQ ID NO: 161)   7 to 26 ACCACTACCT GACCCTGTCC (SEQ ID NO: 162)   6 to 25 CCACTACCTG ACCCTGTCCT (SEQ ID NO: 163)   5 to 24 CACTACCTGA CCCTGTCCTC (SEQ ID NO: 164)   4 to 23 ACTACCTGAC CCTGTCCTCG (SEQ ID NO: 165)   3 to 22 CTACCTGACCC TGTCCTCGA (SEQ ID NO: 166)   2 to 21 TACCTGACCCT GTCCTCGAT (SEQ ID NO: 167)   1 to 20 ACCTGACCCT GTCCTCGATT (SEQ ID NO: 168)

After completion of the DNA template sequence array, the RNA primer consensus sequence (5′-GGACACGGCGAA-3′) (SEQ ID NO:2) was synthesized in close proximity to positions occupied by the previously synthesized DNA template sequences. The RNA primer consensus sequence was synthesized from 5′ to 3′ using 3′-O-DMT-protected 2′-OMe-ribonucleoside phosphoramidites at multiple locations within the array. The newly synthesized RNA primers then hybridized to the DNA template consensus sequence, and served to prime RNA synthesis with T7 RNA polymerase and a DNA sequence template, as shown in FIG. 1. DNA endonuclease, e.g., DNase I, was then used to remove the DNA template from the array to yield the final high density RNA array. The RNA sequences synthesized in array format are shown in Table 2.

The sequences listed below are the RNA sequences enzymatically synthesized on the RNA array. RNA quality control probe 1 (RNA QC1) is the same probe sequence as the fluorescently labeled ssDNA called “ApoE” for quality control purposes. RNA quality control probe 2 (RNA QC2) is the same probe sequence as the fluorescently labeled ssDNA called “w1282” for quality control purposes. RNA quality control probe 3 (RNA QC3) is the complementary sequence to the fluorescently labeled ssDNA called “ApoE” for quality control purposes. RNA quality control probe 4 (RNA QC4) is the complementary sequence to the fluorescently labeled ssDNA called “w1282” for quality control purposes.

The fluorescently labeled “ApoE” ssDNA is capturable to QC3 but not QC 1 in the “tiling RNA array.” The fluorescently labeled “w1282” ssDNA is capturable to QC4 but not QC2 in the “tiling RNA array.”

TABLE 2 IGFBP1 promoter tiling RNA array oligo- nucleotide sequences. (Note: The oligo- nucleotides were sequentially arranged on the tiling array in a clockwise order beginning at the center. The duplicate was arranged into the tiling array afterward.) Name/Position RNA Sequence (5′-->3′) Blank RNA QC1 GCCGAUGACCUGCAAGAGU (SEQ ID NO: 169) RNA QC2 AUAACUUUGCAACAGUGG (SEQ ID NO: 170) RNA QC3 ACUCUUGCAGGUCAUCGGC (SEQ ID NO: 171) RNA QC4 CCACUGUUGCAAAGUUAU (SEQ ID NO: 172) 180 to 161 UAUGAAGGGCUGGCUGUGCG (SEQ ID NO: 173) 179 to 160 AUGAAGGGCUGGCUGUGCGG (SEQ ID NO: 174) 178 to 159 UGAAGGGCUGGCUGUGCGGC (SEQ ID NO: 175) 177 to 158 GAAGGGCUGGCUGUGCGGCA (SEQ ID NO: 176) 176 to 157 AAGGGCUGGCUGUGCGGCAC (SEQ ID NO: 177) 175 to 156 AGGGCUGGCUGUGCGGCACA (SEQ ID NO: 178) 174 to 155 GGGCUGGCUGUGCGGCACAG (SEQ ID NO: 179) 173 to 154 GGCUGGCUGUGCGGCACAGG (SEQ ID NO: 180) 172 to 153 GCUGGCUGUGCGGCACAGGU (SEQ ID NO: 181) 171 to 152 CUGGCUGUGCGGCACAGGUU (SEQ ID NO: 182) 170 to 151 UGGCUGUGCGGCACAGGUUA (SEQ ID NO: 183) 169 to 150 GGCUGUGCGGCACAGGUUAA (SEQ ID NO: 184) 168 to 149 GCUGUGCGGCACAGGUUAAU (SEQ ID NO: 185) 167 to 148 CUGUGCGGCACAGGUUAAUG (SEQ ID NO: 186) 166 to 147 UGUGCGGCACAGGUUAAUGA (SEQ ID NO: 187) 165 to 146 GUGCGGCACAGGUUAAUGAU (SEQ ID NO: 188) 164 to 145 UGCGGCACAGGUUAAUGAUU (SEQ ID NO: 189) 163 to 144 GCGGCACAGGUUAAUGAUUG (SEQ ID NO: 190) 162 to 143 CGGCACAGGUUAAUGAUUGU (SEQ ID NO: 191) 161 to 142 GGCACAGGUUAAUGAUUGUC (SEQ ID NO: 192) 160 to 141 GCACAGGUUAAUGAUUGUCA (SEQ ID NO: 193) 159 to 140 CACAGGUUAAUGAUUGUCAG (SEQ ID NO: 194) 158 to 139 ACAGGUUAAUGAUUGUCAGG (SEQ ID NO: 195) 157 to 138 CAGGUUAAUGAUUGUCAGGG (SEQ ID NO: 196) 156 to 137 AGGUUAAUGAUUGUCAGGGC (SEQ ID NO: 197) 155 to 136 GGUUAAUGAUUGUCAGGGCA (SEQ ID NO: 198) 154 to 135 GUUAAUGAUUGUCAGGGCAG (SEQ ID NO: 199) 153 to 134 UUAAUGAUUGUCAGGGCAGC (SEQ ID NO: 200) 152 to 133 UAAUGAUUGUCAGGGCAGCG (SEQ ID NO: 201) 151 to 132 AAUGAUUGUCAGGGCAGCGU (SEQ ID NO: 202) 150 to 131 AUGAUUGUCAGGGCAGCGUG (SEQ ID NO: 203) 149 to 130 UGAUUGUCAGGGCAGCGUGC (SEQ ID NO: 204) 148 to 129 GAUUGUCAGGGCAGCGUGCU (SEQ ID NO: 205) 147 to 128 AUUGUCAGGGCAGCGUGCUA (SEQ ID NO: 206) 146 to 127 UUGUCAGGGCAGCGUGCUAG (SEQ ID NO: 207) 145 to 126 UGUCAGGGCAGCGUGCUAGG (SEQ ID NO: 208) 144 to 125 GUCAGGGCAGCGUGCUAGGA (SEQ ID NO: 209) 143 to 124 UCAGGGCAGCGUGCUAGGAC (SEQ ID NO: 210) 142 to 123 CAGGGCAGCGUGCUAGGACC (SEQ ID NO: 211) 141 to 122 AGGGCAGCGUGCUAGGACCC (SEQ ID NO: 212) 140 to 121 GGGCAGCGUGCUAGGACCCC (SEQ ID NO: 213) 139 to 120 GGCAGCGUGCUAGGACCCCA (SEQ ID NO: 214) 138 to 119 GCAGCGUGCUAGGACCCCAG (SEQ ID NO: 215) 137 to 118 CAGCGUGCUAGGACCCCAGU (SEQ ID NO: 216) 136 to 117 AGCGUGCUAGGACCCCAGUG (SEQ ID NO: 217) 135 to 116 GCGUGCUAGGACCCCAGUGU (SEQ ID NO: 218) 134 to 115 CGUGCUAGGACCCCAGUGUU (SEQ ID NO: 219) 133 to 114 GUGCUAGGACCCCAGUGUUC (SEQ ID NO: 220) 132 to 113 UGCUAGGACCCCAGUGUUCA (SEQ ID NO: 221) 131 to 112 GCUAGGACCCCAGUGUUCAA (SEQ ID NO: 222) 130 to 111 CUAGGACCCCAGUGUUCAAA (SEQ ID NO: 223) 129 to 110 UAGGACCCCAGUGUUCAAAA (SEQ ID NO: 224) 128 to 109 AGGACCCCAGUGUUCAAAAU (SEQ ID NO: 225) 127 to 108 GGACCCCAGUGUUCAAAAUA (SEQ ID NO: 226) 126 to 107 GACCCCAGUGUUCAAAAUAA (SEQ ID NO: 227) 125 to 106 ACCCCAGUGUUCAAAAUAAG (SEQ ID NO: 228) 124 to 105 CCCCAGUGUUCAAAAUAAGU (SEQ ID NO: 229) 123 to 104 CCCAGUGUUCAAAAUAAGUU (SEQ ID NO: 230) 122 to 103 CCAGUGUUCAAAAUAAGUUU (SEQ ID NO: 231) 121 to 102 CAGUGUUCAAAAUAAGUUUG (SEQ ID NO: 232) 120 to 101 AGUGUUCAAAAUAAGUUUGU (SEQ ID NO: 233) 119 to 100 GUGUUCAAAAUAAGUUUGUU (SEQ ID NO: 234) 118 to 99 UGUUCAAAAUAAGUUUGUUU (SEQ ID NO: 235) 117 to 98 GUUCAAAAUAAGUUUGUUUU (SEQ ID NO: 236) 116 to 97 UUCAAAAUAAGUUUGUUUUG (SEQ ID NO: 237) 115 to 96 UCAAAAUAAGUUUGUUUUGC (SEQ ID NO: 238) 114 to 95 CAAAAUAAGUUUGUUUUGCU (SEQ ID NO: 239) 113 to 94 AAAAUAAGUUUGUUUUGCUU (SEQ ID NO: 240) 112 to 93 AAAUAAGUUUGUUUUGCUUG (SEQ ID NO: 241) 111 to 92 AAUAAGUUUGUUUUGCUUGU (SEQ ID NO: 252) 110 to 91 AUAAGUUUGUUUUGCUUGUG (SEQ ID NO: 243) 109 to 90 UAAGUUUGUUUUGCUUGUGA (SEQ ID NO: 244) 108 to 89 AAGUUUGUUUUGCUUGUGAG (SEQ ID NO: 245) 107 to 88 AGUUUGUUUUGCUUGUGAGC (SEQ ID NO: 246) 106 to 87 GUUUGUUUUGCUUGUGAGCU (SEQ ID NO: 247) 105 to 86 UUUGUUUUGCUUGUGAGCUC (SEQ ID NO: 248) 104 to 85 UUGUUUUGCUUGUGAGCUCU (SEQ ID NO: 249) 103 to 84 UGUUUUGCUUGUGAGCUCUA (SEQ ID NO: 250) 102 to 83 GUUUUGCUUGUGAG CUCUAC (SEQ ID NO: 250) 101 to 82 UUUUGCUUGUGAGC UCUACA (SEQ ID NO: 252) 100 to 81 UUUGCUUGUGAGCU CUACAC (SEQ ID NO: 253)  99 to 80 UUGCUUGUGAGCUC UACACA (SEQ ID NO: 254)  98 to 79 UGCUUGUGAGCUCU ACACAA  97 to 78 GCUUGUGAGCUCUAC ACAAA (SEQ ID NO: 255)  96 to 77 CUUGUGAGCUCUACA CAAAC (SEQ ID NO: 256)  95 to 76 UUGUGAGCUCUACAC AAACC (SEQ ID NO: 257)  94 to 75 UGUGAGCUCUACACA AACCG (SEQ ID NO: 258)  93 to 74 GUGAGCUCUACACAA ACCGU (SEQ ID NO: 259)  92 to 73 UGAGCUCUACACAAA CCGUG  91 to 72 GAGCUCUACACAAAC CGUGG (SEQ ID NO: 260)  90 to 71 AGCUCUACACAAACC GUGGG (SEQ ID NO: 261)  89 to 70 GCUCUACACAAACCG UGGGU (SEQ ID NO: 262)  88 to 69 CUCUACACAAACCGU GGGUG (SEQ ID NO: 263)  87 to 68 UCUACACAAACCGUG GGUGG (SEQ ID NO: 264)  86 to 67 CUACACAAACCGUGG GUGGA (SEQ ID NO: 265)  85 to 66 UACACAAACCGUGGG UGGAA (SEQ ID NO: 266)  84 to 65 ACACAAACCGUGGGU GGAAG (SEQ ID NO: 267)  83 to 64 CACAAACCGUGGGUG GAAGG (SEQ ID NO: 268)  82 to 63 ACAAACCGUGGGUG GAAGGG (SEQ ID NO: 269)  81 to 62 CAAACCGUGGGUGG AAGGGG (SEQ ID NO: 270)  80 to 61 AAACCGUGGGUGGA AGGGGG (SEQ ID NO: 271)  79 to 60 AACCGUGGGUGGAA GGGGGU (SEQ ID NO: 272)  78 to 59 ACCGUGGGUGGAAG GGGGUA (SEQ ID NO: 273)  77 to 58 CCGUGGGUGGAAGG GGGUAA (SEQ ID NO: 274)  76 to 57 CGUGGGUGGAAGGG GGUAAA (SEQ ID NO: 275)  75 to 56 GUGGGUGGAAGGGG GUAAAG (SEQ ID NO: 276)  74 to 55 UGGGUGGAAGGGGG UAAAGG (SEQ ID NO: 277)  73 to 54 GGGUGGAAGGGGGU AAAGGG (SEQ ID NO: 278)  72 to 53 GGUGGAAGGGGGUA AAGGGA  71 to 52 GUGGAAGGGGGUAA AGGGAU (SEQ ID NO: 279)  70 to 51 UGGAAGGGGGUAAA GGGAUC (SEQ ID NO: 280)  69 to 50 GGAAGGGGGUAAAG GGAUCA (SEQ ID NO: 281)  68 to 49 GAAGGGGGUAAAGG GAUCAG (SEQ ID NO: 282)  67 to 48 AAGGGGGUAAAGGG AUCAGG (SEQ ID NO: 283)  66 to 47 AGGGGGUAAAGGGA UCAGGU (SEQ ID NO: 284)  65 to 46 GGGGGUAAAGGGAU CAGGUU (SEQ ID NO: 285)  64 to 45 GGGGUAAAGGGAUC AGGUUU (SEQ ID NO: 286)  63 to 44 GGGUAAAGGGAUCA GGUUUU (SEQ ID NO: 287)  62 to 43 GGUAAAGGGAUCAG GUUUUC (SEQ ID NO: 288)  61 to 42 GUAAAGGGAUCAGG UUUUCU (SEQ ID NO: 289)  60 to 41 UAAAGGGAUCAGGU UUUCUA (SEQ ID NO: 290)  59 to 40 AAAGGGAUCAGGUU UUCUAC (SEQ ID NO: 291)  58 to 39 AAGGGAUCAGGUUU UCUACU (SEQ ID NO: 292)  57 to 38 AGGGAUCAGGUUUU CUACUA (SEQ ID NO: 293)  56 to 37 GGGAUCAGGUUUUC UACUAU (SEQ ID NO: 294)  55 to 36 GGAUCAGGUUUUCU ACUAUG (SEQ ID NO: 295)  54 to 35 GAUCAGGUUUUCUA CUAUGU (SEQ ID NO: 296)  53 to 34 AUCAGGUUUUCUAC UAUGUU (SEQ ID NO: 297)  52 to 33 UCAGGUUUUCUACU AUGUUU (SEQ ID NO: 298)  51 to 32 CAGGUUUUCUACUA UGUUUG (SEQ ID NO: 299)  50 to 31 AGGUUUUCUACUAU GUUUGU  49 to 30 GGUUUUCUACUAUG UUUGUC (SEQ ID NO: 300)  48 to 29 GUUUUCUACUAUGU UUGUCC (SEQ ID NO: 301)  47 to 28 UUUUCUACUAUGUU UGUCCC (SEQ ID NO: 302)  46 to 27 UUUCUACUAUGUUU GUCCCG (SEQ ID NO: 303)  45 to 26 UUCUACUAUGUUUG UCCCGU (SEQ ID NO: 304)  44 to 25 UCUACUAUGUUUGU CCCGUG (SEQ ID NO: 305)  43 to 24 CUACUAUGUUUGUCC CGUGG (SEQ ID NO: 306)  42 to 23 UACUAUGUUUGUCCC GUGGU (SEQ ID NO: 307)  41 to 22 ACUAUGUUUGUCCCG UGGUG (SEQ ID NO: 308)  40 to 21 CUAUGUUUGUCCCGU GGUGA (SEQ ID NO: 309)  39 to 20 UAUGUUUGUCCCGU GGUGAU (SEQ ID NO: 310)  38 to 19 AUGUUUGUCCCGUG GUGAUG (SEQ ID NO: 311)  37 to 18 UGUUUGUCCCGUGG UGAUGG (SEQ ID NO: 312)  36 to 17 GUUUGUCCCGUGGU GAUGGA (SEQ ID NO: 313)  35 to 16 UUUGUCCCGUGGUG AUGGAC (SEQ ID NO: 314)  34 to 15 UUGUCCCGUGGUGA UGGACU (SEQ ID NO: 315)  33 to 14 UGUCCCGUGGUGAU GGACUG (SEQ ID NO: 316)  32 to 13 GUCCCGUGGUGAUG GACUGG (SEQ ID NO: 317)  31 to 12 UCCCGUGGUGAUGG ACUGGG (SEQ ID NO: 318)  30 to 11 CCCGUGGUGAUGGAC UGGGA (SEQ ID NO: 319)  29 to 10 CCGUGGUGAUGGAC UGGGAC (SEQ ID NO: 320)  28 to 9 CGUGGUGAUGGACU GGGACA (SEQ ID NO: 321)  27 to 8 GUGGUGAUGGACUG GGACAG (SEQ ID NO: 322)  26 to 7 UGGUGAUGGACUGG GACAGG (SEQ ID NO: 323)  25 to 6 GGUGAUGGACUGGG ACAGGA (SEQ ID NO: 324)  24 to 5 GUGAUGGACUGGGA CAGGAG (SEQ ID NO: 325)  23 to 4 UGAUGGACUGGGAC AGGAGC (SEQ ID NO: 326)  22 to 3 GAUGGACUGGGACA GGAGCU (SEQ ID NO: 327)  21 to 2 AUGGACUGGGACAG GAGCUA (SEQ ID NO: 328)  20 to 1 UGGACUGGGACAGG AGCUAA (SEQ ID NO: 329)

The oligonucleotides were sequentially arranged on the tiling array in a clockwise order beginning at the center (FIG. 2). The duplicate was arranged into the tiling array afterward.

In order to generate a probe to test the presence of RNA sequences in the array, two units of T7 exonuclease were used to digest 100 ng of one end FAM-labeled and 5′ phosphorothioate-protected IGFBP1 DNA for 1 min at room temperature. T7 exonuclease digestion was stopped by addition of EDTA to a final concentration of 25 mM. The product was applied onto the RNA array for hybridization at 37° C. for 1 hr.

The fluorescence signal that is observed arises from a sequence-specific capture of partial duplex DNA that was fluorescently tagged (6-carboxyfluorescein, FAM) and protected by phosphorothioate DNA bases at its 5′ end (FIG. 2A). Fluorescence signal from each array element provides a measurement of the amount of digested duplex capturable by specific complementary oligonucleotides and was expected to vary with the degree of digestion. We profiled the digestion characteristics of T7 exonuclease on FAM labeled 180 bp long IGFBP1 DNA in a control condition (2 units of T7 exonuclease on 100 ng IGFBP1 DNA at room temperature for 1 min) by using the RNA tiling arrays (FIG. 2B). The target DNA was captured in a sequence-specific manner. It is noted that the digestion activity of T7 exonuclease is similar to the activity of Exonuclease 3 (3′ DNA exonuclease) that was reported previously Wu et al (2011), PLoS One 6, e26217. The result suggests the desired RNA sequences were synthesized accurately on the surface and are accessible for sequence-specific capture of nucleic acids.

In summary, we demonstrated here a strategy for making high density RNA arrays by taking advantage of well-developed DNA array technology. Using this method, millions of RNA oligonucleotides can be copied from high density DNA microarray templates simultaneously with this method. The enzymatically synthesized RNAs on the surface are free from undesired chemical modifications that are inevitable during chemical syntheses resulting from long time exposures to strong acidic and oxidizing reagents. Also, this method is not constrained by the relatively lower coupling yield of RNA phosphoramidites (compared to DNA), and the laborious process for chemical RNA synthesis. Furthermore, modified ribonucleoside triphosphates (e.g., 2′-fluorine-CTP or 2′-fluorine-UTP) can be used to fabricate desired RNA arrays for various applications. High density RNA arrays provide a new avenue for high throughput RNA biomolecular interaction analyses and RNA research.

Example 2 RNA Arrays Synthesized with 2′-Fluoro Ribonucleosides are RNase-Resistant

In order to determine if RNA arrays could be generated that were RNase resistant, an RNA array and a 2′-fluoro-RNA array were enzymatically synthesized as described previously using natural nucleoside triphosphates (i.e., adenosine triphosphate [ATP], guanosine triphosphate [GTP], cytidine triphosphate [CTP], and uridine triphosphate [UTP] and 2′ fluorine modified nucleoside triphosphate mix (i.e. adenosine triphosphate [ATP], guanosine triphosphate [GTP], 2′-fluoro-2′ deoxycytidine triphosphate [2′-F-dCTP], 2′-fluoro-2′ deoxyuridine triphosphate [2′-F-dUTP]), respectively. Both RNA arrays were then treated with DNase I (20 units) at 37° C. for four hours to eliminate template DNA oligonucleotides, followed by RNase A treatment (>4 units) at 37° C. for 30 minutes. The arrays were then hybridized with their fluorescently labeled cDNAs. As shown in FIG. 3, the RNA arrays generated with unmodified ribonucleotides (upper panels) showed persistent hybridization signal after DNase I treatment, indicating hybridization of the cDNA probe to the RNA array. However, after RNase A treatment, a complete loss of hybridization signal was observed indicating complete degradation of the RNA array. In contrast, the 2′-fluoro-RNA arrays, showed hybridization signal after DNase treatment and RNase A treatment. These data show that the use of RNase-resistant ribonucleosides such as 2′-fluoro ribonucleotides is useful in generating RNase-resistant RNA arrays.

Example 3 Generation of Patterned RNA Arrays Having Functional Properties

We describe here a simple yet powerful new strategy for the enzymatic synthesis of high-density RNA arrays. The key idea is to use RNA polymerase to copy surface-attached DNA molecules on a high-density DNA array into their RNA complements (FIG. 1). The surface is first partially deprotected (e.g. light is used to effect removal of 50% of the NPPOC photolabile protecting groups covering the surface), an array of the DNA complements to the eventual desired RNA sequences is synthesized by standard light-directed synthesis on the exposed sites, and the remaining surface sites are then deprotected, followed by synthesis of RNA primer sequences. These primer sequences on the second group of sites are hybridized to their complements on the first group, whereupon they may be extended with T7 RNA polymerase to yield RNA:DNA duplexes. The DNAs are removed with DNase I, leaving behind the desired single stranded RNAs. The strategy is compatible with either natural unmodified ribonucleoside triphosphates (rNTPs), or alternatively, 2′ fluoro-modified (2′F) rNTPs may be included in the polymerase extension reaction to impart nuclease resistance and other desirable characteristics to the synthesized RNAs. We note that the use of a very long, flexible, hydrophilic spacer (we employed a PEG 2000 moiety) between the substrate and the oligonucleotides is critical—this is not surprising, as it is necessary for the DNA complement and RNA primer sequences to anneal while both are still attached to the surface. A second key to this strategy is the ability to fabricate two different nucleic acid sequences within individual DNA features—in this case, both a primer sequence, and a template sequence.

Methods Array Substrate Preparation

Standard glass slides coated with 50 Å chromium and 1,000 Å of gold (EMF corp., NY, USA) were extensively rinsed with hexane and ethanol and dried under a nitrogen stream. A 7.5 nm layer of amorphous carbon was then DC magnetron sputtered on the gold surface (Denton Vacuum, NJ, USA). The carbon-on-gold surface was hydrogen-terminated in a 13.56 MHz inductively coupled hydrogen plasma for 12 minutes (30 Torr H₂, room temperature). Next, 40 μA of 9-Decene-1-ol (Sigma Aldrich, MO, USA) was placed directly onto the newly hydrogen-terminated surface and covered with a quartz coverslip. The surfaces were irradiated under nitrogen purge with a low-pressure mercury vapor quartz grid lamp (X=254 nm, 0.35 mW/cm²) for 16 h. After the photoreaction, the surfaces were rinsed extensively with ethanol and deionized water and dried under a nitrogen stream.

In Situ Oligonucleotide Array Synthesis

Light-directed photolithographic synthesis of DNA template arrays was performed on a 9-Decen-1-ol modified carbon-on-gold surface with a digital micromirror-based Maskless Array Synthesis (MAS) system connected to an ABI Expedite™ 8909 Nucleic Acid Synthesis System (Applied Biosystems, CA, USA) as described previously. All the 5′-NPPOC-protected phosphoramidite nucleosides underwent a single 80 sec coupling step. All the 3′-dimethoxytrityl (DMT)-protected phosphoramidite nucleosides underwent a single 360 sec coupling step. The 5′-DMT-protected polyethyleneglycol 2000 phosphoramidite underwent two 900 sec coupling steps in a row. While the NPPOC protecting groups were removed by exposure to UV light, all the DMT protecting groups were removed by flowing through a deblocking mix (3% dichloroacetic acid in toluene). The light dose to remove full or a half of the photolabile NPPOC (nitrophenylpropyloxycarbonyl) protecting groups was determined prior to DNA template array fabrication. A series of incremental doses of 365 nm light (Joule/cm²) was used for a 30 nt quality control (QC) oligonucleotide synthesis. The optimal dose was chosen to yield the highest level of fluorescence (for a full deprotection) or a half of it (for a half deprotection) from hybridization of a fluorescently tagged QC complement. A total dose of 3 Joule/cm² 365 nm light was used to remove all NPPOCs during each cycle. A total dose of 0.32 Joule/cm² 365 nm light was used to remove a half of NPPOCs for RNA primer synthesis. After half-deprotection of the first layer of NPPOC-protected phosphoramidite nucleosides, the exposed hydroxyl moieties were reacted with the DMT-protected phosphoramidite nucleosides at the first base of the RNA primer. Afterward, the other half of the NPPOC protecting groups were removed by a full dose of UV light prior to the light-directed oligonucleotide synthesis on the surface. After the light-directed oligonucleotide synthesis of DNA template was completed, the 5′ end of the oligodeoxyribonucleotides were capped three times with a 1:1 v/v mixture of capping reagents A and B (A:B solution; see below) for 90 sec (˜320 μl). The DMT protecting groups on the first base of RNA primer were removed using a deblocking mix, and the RNA primer sequence was synthesized using a standard nucleic acid synthesis protocol. DCI Activator (0.25 M dicyanoimidazole in acetonitrile) and all NPPOC (3′-nitrophenylpropyloxycarbonyl) protected phosphoramidite nucleosides [5′-NPPOC-dAdenosine (tac) 3′-β-cyanoethylphosphoramidite (NPPOC-dA), 5′-NPPOC-dThymidine 3′-β-cyanoethylphosphoramidite (NPPOC-dT), 5′-NPPOC-dCytidine (ib) 3′-β-cyanoethylphosphoramidite (NPPOC-dC), 5′-NPPOC-dGuanosine (ipac) 3′-β-cyanoethylphosphoramidite (NPPOC-dG)], N-methylimidazole, acetonitrile, and tetrahydrofuran (THF) were purchased from Sigma Aldrich (MO, USA). Capping reagent A (THF/PAc2O) and deblocking mix were purchased from Glen Research (VA, USA). Oxidation solution (0.02 M iodine/pyridine/H₂O/THF), acetonitrile anhydrous, 5′-DMT-polyethyleneglycol 2000 phosphoramidite, all 3′-DMT-5′-cyanoethylphosphoramite 2′-O-methyl or 2′-fluoro nucleosides were purchased from ChemGenes (MA, USA). Capping reagent B (6.5% 2-dimethylaminopyridine, 2% N-methylimidazole and 10% 2,6-lutidine in THF) and exposure solvent (1% imidazole in DMSO) were mixed in-house Anhydrous reagents were kept over molecular sieves (AldraSORB™ water trapping packets, Sigma Aldrich).

Enzymatic Fabrication of RNA Arrays

A gasket, Gene Frame—1×1 cm internal (Abgene, Epsom, UK), was attached so that it surrounds the DNA features. A 50 μl annealing buffer consisting of 4×SSPE buffer (Sigma Aldrich), 1× RNasecure™ reagent (Ambion, TX, USA), 9% polyethylene glycol 6000, was applied onto the array and incubated at 60° C. for 20 min, then slowly cooled down to 37° C. for 4 hr. The prolonged incubation time allows the RNA primers to anneal adequately to their DNA complements. The polyethylene glycol accelerated RNA:DNA hybridization while RNasecure™ was included to irreversibly inactivate possible RNases on the surface. The surface was rinsed with 1× transcription buffer (40 mM Tris-HCl, pH 7.9, 6 mM MgCl₂, 10 mM DTT, 20 mM NaCl, 2 mM spermidine) prior to RNA extension reaction. For 2′-fluoro RNA extension, a mutant T7 RNA polymerase was used while wild-type T7 RNA polymerase was used for natural RNA extension. A 50 μA RNA extension reaction mixture was added to the surface and incubated at 37° C. for 6-8 h in a humid chamber. A natural RNA extension reaction mixture consists of 40 mM Tris-HCl, pH 7.9, 6 mM MgCl₂, 10 mM DTT, 20 mM NaCl, 2 mM spermidine, 0.5 mM each NTP, 2 U/μl T7 RNA polymerase (Thermo Scientific, USA), and 1 U/μl RNase inhibitor (New England Biolabs, USA). A 2′-fluoro RNA extension reaction mixture consists of 40 mM Tris-HCl, pH 7.9, 2 mM MgCl₂, 2 mM MnCl₂, 10 mM DTT, 20 mM NaCl, 0.05% Triton X-100, 012 mg/μl BSA, 2 mM spermidine, 0.5 mM adenosine triphosphate, 0.5 mM guanosine triphosphate, 0.5 mM 2′-fluoro-uridine triphosphate (TriLink, CA, USA), 0.5 mM 2′-fluoro-cytidine triphosphate (TriLink), 0.015 U/μl pyrophosphatase, 2 U/μl T7 R&DNA polymerase (Epicentre, WI, USA) and 1 U/μl RNase inhibitor (New England Biolabs, USA). After extension reaction, CaCl₂ was added to a final concentration of 0.5 mM, and Turbo DNase (Ambion, TX, USA) was added to a final concentration of 0.1 U/μl. The reaction mixture was incubated at 37° C. for another 6˜8 h to completely remove the DNA templates in a humid chamber. The resulting array was immersed in TE buffer, pH 7.0 at 75° C. for 10 min to inactivate DNase I and T7 RNA polymerase. The array was rinsed extensively with TE buffer and deionized water and dried under a nitrogen stream.

Capture and Detection of Fluorescently Labeled DNA on High Density RNA Arrays

The fluorescein labeled DNA fragment corresponding to positions −205 to −25 of the mouse IGFBP1 promoter was amplified by PCR from NIH 3T3 (mouse embryonic fibroblast cell line) genomic DNA (NEB, MA, USA) using the primers (5′-T*T*A GC/iFluorT/ CCT GTC CCA GTC CAT-3′ (SEQ ID NO:4) and 5′-TAT GAA GGG CTG GCT GTG C-3′ (SEQ ID NO:5). [*] represents a phosphorothioate DNA base and [/iFluorT/] represents a fluorescein-labeled thymidine. All primers were custom synthesized by IDT (Integrated DNA Technologies, IA, USA). AmpliTaq DNA polymerase (Applied Biosystems, CA, USA) was used in the PCR reaction. The PCR cycling consisted of 3 min at 94° C.; then 40 cycles of 30 sec at 95° C., 30 sec at 59° C., and 30 sec at 72° C.; and final elongation 6 min at 72° C. The amplicon was purified using the Promega Wizard SV Gel and PCR Clean-up System (Promega, WI, USA). A total of 720 ng of purified PCR amplicion was partially digested with 15 units of T7 exonuclease (T7 Gene 6 Exonuclease; Affymetrix, CA, USA) at 25° C. for 1 min and right away quenched with EDTA at a final concentration of 25 mM.

Following inactivation of the T7 exonuclease at 75° C. for 10 min, the reaction buffer was exchanged to 1×SSPE buffer at a concentration of 0.2 μM before application to the RNA arrays. The hybridization reaction was performed in a humid chamber at 25° C. for 30 min, followed by a thorough rinse and incubation with 1×SSPE buffer at 37° C. for 15 min to remove nonspecifically bound DNA. Fluorescence images were obtained with a 488 nm laser and 512 nm filter using a GeneTac UC 4×4 microarray scanner (Genomic Solutions, MI, USA). Table 1 contains the probe sequences synthesized on the surface. Each of the tiling arrays was composed of 332 features with each feature measuring 280 μm×280 μm, and separated by 140 μm gaps.

Nuclease Susceptibility Test

DNase I (Turbo DNase; Ambion) and RNase A (Ribonuclease A; Sigma Aldrich) were used to interrogate the nature of DNA, RNA and 2′-fluoro RNA “Badger Chemist” arrays. All arrays were first hybridized with a mixture of three fluorescently labeled DNA probes and visualized using a GeneTac UC 4×4 microarray scanner. The hybridization reaction mixture consisted of 0.2 μM of each probe in 4×SSPE buffer and was incubated in a humid chamber at 37° C. for 30 min, followed by a thorough rinse and incubation with 1× SSPE buffer at 37° C. for 15 min to remove nonspecifically bound DNA. Table 3 contains the sequences of a “Badger Chemist” array, as well as the fluorescently labeled detection probes. The RNA and 2′-fluoro RNA arrays were first treated with a total of 2.5 units of DNase I at 37° C. for 7 hr and then a total of 1 μg of RNase A. Conversely, the DNA arrays were first treated with RNase A and then with DNase I. The arrays were heat treated at 75° C. for 10 min before again being subjected to fluorescence imaging.

TABLE 3 Badger Chemist DNA and RNA Array Sequences (see FIG. 4) Badger Chemist DNA Expected Badger Chemist template array sequences RNA array Sequences Name Sequence (3′ to 5′) Name Sequence (5′ to 3′) body TGAGAACGTCCAGTAGCCG body ACUCUUGCAGGUCAUCGGC (SEQ ID NO: 10) (SEQ ID NO: 171) lab coat GATTGTCCACTCAAGACT lab coat CUAACAGGUGAGUUCUGA (SEQ ID NO: 330) (SEQ ID NO: 331) sweater/flask GGTGACAACGTTTCAATA sweater/flask CCACUGUUGCAAAGUUAU (SEQ ID NO: 11) (SEQ ID NO: 172)

The sequence initiated from the surface for the Badger Chemist template DNA array is 3′-T/PEG2K/A GCC TGT GCC GCT T-5′ (SEQ ID NO:332); and the sequence initiated from the surface for the Badger Chemist RNA tiling array is 5′-T/PEG2K/A fCmG mG mAfCmAfC mGmGfC mGmAmA-3,′ which served as an RNA primer for extension reaction. Italic letters represent RNA bases./PEG2K/ represents a polyethylene glycol linker of an approximate molecular weight of 2,000 Da. mG and mA are 2′-methoxy RNA bases. fC is a 2′-fluoro RNA base.

24-2-min aptamer binding assay

An RNA array consisting of the 24-2-min sequence (5′-mGmAfC mGfCmG mAfCfC mGmAmA AUG GUG AAG GAC GGG UCC AGU GCU UCG GCA CUG UUG AGU AGA GUG UGA GCU CCG UAA CUG GUC GCG UC-3′ (SEQ ID NO:333) in the pattern of the University Wisconsin logo was used for a functional assay. [m] represents a “2′-methoxy” RNA base, while [f] represents “2′-fluoro” RNA base. The underscored sequence is the RNA primer sequence synthesized using DMT-protected phosphoramidite nucleosides. The array was heat denatured at 75° C. for 5 min and quickly chilled on ice in a binding buffer containing 40 mM HEPES pH 7.4, 125 mM KCl, 5 mM MgCl₂, and 5% DMSO. The array was then incubated with DFHBI at a final concentration of 20 μM for 30 min at room temperature. The image was visualized under a 488 nm laser with a 512 nm filter using a GeneTac UC 4×4 microarray scanner.

Cleavage Tests with 10-23 DNAZyme

Table 3 contains the sequences of a “Badger Chemist” array. The 10-23 DNAZyme (5′-TCA GAA CTC AGG CTA GCT ACA ACG ACT GTT AGT TC-3′) (SEQ ID NO:334) is designed to cleave the “lab coat” RNA sequence in the “Badger Chemist” array). The underscored sequences are the substrate-binding domains. The arrays were first annealed with the 10-23 DNAzyme at a final concentration of 1 μM in a 50 μl annealing buffer (5 mM Tris, pH 7.5, 15 mM NaCl, 0.1 mM EDTA). After application of the mixture to the array, the surface was incubated on a heating block at 95° C. for 3 min following by chilling on ice. The cleavage reaction was initiated by addition of 10× cleavage buffer followed by 10×Mn²⁺ to give a final incubation condition of 50 mM Tris, pH 7.5, 10 mM MnCl₂, and 150 mM NaCl. The sample was placed in a humid chamber at 37° C. for 5 hr for DNAZyme cleavage and immersed in 8 M urea solution to stop the reaction. Both before and after DNAZyme treatment, the arrays were hybridized with a mixture of three fluorescently labeled DNA probes and visualized using a GeneTac UC 4×4 microarray scanner.

Several approaches were employed to evaluate the fidelity and utility of the arrays: these include nuclease sensitivity, DNA hybridization, DNAzyme cleavage, and RNA aptamer binding experiments. FIG. 4 shows the results of nuclease digestion experiments on DNA, RNA, and 2′F RNA arrays. Each array contains three 30-32mer sequences corresponding to the body, sweater/flask, or lab coat of a “Badger Chemist” (Table 3). The arrays were visualized after nuclease treatment by hybridizing them with a mixture of the three corresponding oligodeoxynucleotide complements, tagged respectively with the fluorophores fluorescein (sweater and bag), Texas Red (head; hands; and feet), and Cy 5 (labcoat), followed by washing and fluorescence imaging. It is evident from the figure that while the DNA arrays are completely destroyed by DNase treatment but impervious to RNase treatment, the RNA arrays show the opposite result, in that they are completely destroyed by RNase treatment but impervious to DNase treatment. As expected, the 2′F RNA arrays are resistant to both DNase and RNase treatment. These results confirm in each case the nature of the nucleic acid comprising the array elements. In addition, the experiments also show that for each array, the nucleic acid molecules on the surface hybridize specifically to fluorescently tagged solution complements, as illustrated by the correct localization of the green, yellow, and red features in the image.

The hybridization and exonuclease sensitivity results presented in Example 1 above and in this example provide strong evidence that the normal and modified RNA arrays have the correct nucleic acid compositions, and exhibit normal base-pairing functionality. We sought to further confirm the functionality of the sequences with two additional experiments: the ability of the RNA sequences to serve as substrates for a RNA-specific DNAzyme, and their ability to fold correctly into RNA aptamers and exhibit specific binding to a target molecule.

The 10-23 DNAzyme (having RNase activity), first described by Joyce and colleagues in 1997 (Santoro et al, 1997, Proc Natl Acad Sci USA. 94(9):4262-4266), consists of a catalytic core of 15 deoxynucleotides flanked by substrate-binding domains. Any RNA substrate that is accessible to Watson-Crick pairing with the 10-23 DNAzyme substrate-binding domains can be cleaved at the phosphodiester linkage between purine and pyrimidine nucleobases that separate the complementary regions on the substrate (FIG. 5A). We designed a 10-23 DNAzyme to cleave the RNA sequences on the “Badger Chemist” array that correspond to the lab coat. The arrays were incubated with the 10-23 DNAzyme in a Mn⁺² containing buffer for 5 hr at 37° C. As shown in FIG. 5B, the “lab coat” sequences remained intact on the DNA array, whereas 70% were cleaved on the RNA array and 55% were cleaved on the 2′-fluoro RNA array. These results show that the surface-bound natural and modified RNA molecules are recognized as RNA by the DNAzyme.

One important application of RNA arrays is likely to be their use for the discovery, characterization, and evolution of aptamer sequences. The term “aptamer” refers to nucleic acid molecules that fold into conformations that impart them with specific binding affinity for a molecular target. Although nucleic acid aptamers can be composed of either DNA or RNA, RNA aptamers have the intriguing advantage of being possible to generate in vivo, and in fact naturally occurring RNA aptamers known as “riboswitches” have been described and shown to play critical roles in gene regulation. We wished to determine if the surface-bound RNAs in RNA arrays were able to fold properly to yield functional aptamer sequences. We chose to evaluate the “24-2” aptamer recently developed by Jaffrey and co-workers (Paige et al 2011, Science: 333:642-646). This aptamer imparts fluorescent properties similar to those of green fluorescent protein (GFP) to RNA molecules. It does this by binding the chromophore DFHBI (3,5-difluoro-4-hydroxybenzylidene imidazolinone); although in solution this chromophore is non-fluorescent, when immobilized by binding to the 24-2 aptamer its dihedral freedom is restricted and it becomes fluorescent. As described by Jaffrey and colleagues, if the aptamer sequence is fused with a naturally occurring RNA of interest, addition of DFHBI renders it visible by fluorescence imaging, making it possible to visualize the tagged RNA molecules in living cells. “24-2 min” is a shorter version of the original 24-2 aptamer.

We fabricated an RNA array consisting of the 24-2-min aptamer sequence in the pattern of the University of Wisconsin logo. The array was incubated with DFHBI followed by fluorescence imaging. The fluorescence image in FIG. 6 shows a pattern of green fluorescence corresponding to the logo, demonstrating that the aptamer sequences are properly folded and functional. This result suggests the possibility of synthesizing hundreds of thousands of variant 24-2 sequences on the array, and screening them all in parallel to identify aptamers with improved fluorescence characteristics such as increased brightness or red-shifted fluorescence emission.

In summary, we have described a novel strategy for the fabrication of high-density RNA arrays. The fidelity and functionality of the RNA elements is demonstrated in hybridization, DNAzyme cleavage, nuclease digestion, and RNA aptamer binding experiments. 

What is claimed is:
 1. An RNA array comprising RNAs that (i) are covalently linked at their 5′ ends to a solid support; (ii) represent at least 10 unique RNA sequences; and (iii) have a feature density of at least 20 features/cm².
 2. The RNA array of claim 1, wherein the at least ten unique RNA sequences comprise at least 50 unique RNA sequences.
 3. The RNA array of claim 1, wherein the length of the at least ten unique sequences is about 20 to about 50 bases long.
 4. The RNA array of claim 1, wherein the density of single-stranded RNAs is about 200 features/cm.
 5. The RNA array of claim 1, wherein the RNAs comprise modified ribonucleotides.
 6. The RNA array of claim 5, wherein the modified ribonucleotides are RNase resistant.
 7. A template array comprising an array of (i) single-stranded template DNA oligonucleotides linked at their 3′ ends to a solid support, comprising a consensus sequence, and capped by a protecting group at their 5′ end; and (ii) single-stranded RNA primers that are covalently linked at their 5′ ends to the solid support, and that are complementary to the consensus sequence, wherein the single-stranded RNA primers hybridize to the single-stranded template DNA oligonucleotides.
 8. The template array of claim 7, wherein the single-stranded template DNA oligonucleotides are about 20 bases in length.
 9. The template array of claim 7, wherein the single-stranded RNA primers are about 4 bases to about 20 bases long.
 10. The template array of claim 7, wherein the single-stranded template DNA oligonucleotides or single-stranded RNA primers are covalently linked to the solid support through a polyethylene glycol spacer.
 11. The template array of claim 7, wherein the protecting group is an acetyl group or phenoxyacetyl group.
 12. A kit comprising the template array of claim 7, and any of (i) an RNA polymerase; (ii) ribonucleoside triphosphates; and (iii) a DNase.
 13. The kit of claim 12, wherein the ribonucleoside triphosphates are modified ribonucleoside triphosphates that are RNase-resistant.
 14. A method for generating a template array, comprising (i) providing a solid support comprising a layer of protected deoxyribonucleosides that comprise a 5′-photolabile protecting group and are covalently linked at their 3′ end to a spacer layer bound to the solid support; (ii) irradiating the layer of protected deoxyribonucleosides with ultraviolet energy sufficient to deprotect about half of the protected deoxyribonucleosides; (iii) coupling the deprotected deoxyribonucleosides with a ribonucleoside phosphoramidite comprising a 5′ acid-labile protecting group; (iv) irradiating the remaining protected deoxyribonucleosides with ultraviolet irradiation sufficient to deprotect all of the remaining protected deoxyribonucleosides; (v) extending the deprotected deoxyribonucleosides, at one or more locations, by light-directed 3′ to 5′ photolithographic synthesis to generate template DNA oligonucleotides of the deprotected deoxyribonucleosides; (vi) coupling a protecting group to the 5′ ends of the template DNA oligonucleotides; (vii) removing the 5′ acid-labile protecting group on the protected ribonucleosides by acid treatment; and (viii) extending the deprotected ribonucleosides at one or more locations, by 5′ to 3′ chemical synthesis of RNA primers comprising a sequence that is complementary to a sequence at the 3′ end of the template DNA strands to obtain a template array.
 15. The method of claim 14, wherein in step (iii) the 5′ acid-labile protecting group comprises a 4,4′-dimethoxytrityl (DMT) group.
 16. The method of claim 14, wherein in step (vi) the protecting group coupled to the 5′-ends of the template DNA strands is an acetyl group or phenoxyacetyl group.
 17. The method of claim 14, wherein in step (viii) RNase-resistant modified ribonucleoside phosphoramidites are used in the extension of the deprotected phosphoramidites to obtain RNase-resistant RNA primers.
 18. The method of claim 17, wherein the RNase-resistant modified ribonucleoside phosphoramidites are 2′-fluoro ribonucleoside phosphoramidites or 2′-methoxy ribonucleoside phosphoramidites.
 19. A method for generating an RNA array, comprising (i) providing: a template array of (a) single-stranded template DNAs linked at their 3′ end to a solid support and comprising a consensus sequence; and (b) single-stranded RNA primers that are covalently linked at their 5′ end to the solid support, and that are complementary to the consensus sequence of the single-stranded template DNAs; (ii) hybridizing the single-stranded RNA primers with the single-stranded template DNAs; (iii) extending the hybridized RNA primers along the single-stranded template DNAs using an RNA polymerase and ribonucleoside triphosphates to obtain double-stranded DNA-RNA hybrids; and (iv) contacting the DNA-RNA hybrids with a DNase to remove the template DNAs from the DNA-RNA hybrids to obtain an RNA array.
 20. The method of claim 19, wherein the RNA polymerase in step (iii) is T7 RNA polymerase.
 21. The method of claim 19, wherein the ribonucleoside triphosphates are modified ribonucleoside triphosphates.
 22. The method of claim 21, wherein the modified ribonucleoside triphosphates are RNase resistant modified ribonucleoside triphosphates.
 23. The method of claim 19, further comprising synthesizing the single-stranded RNA primers in the array prior to step (i).
 24. The method of claim 19, wherein the single-stranded template DNAs represent at least 50 unique sequences.
 25. A method to generate an RNA bead pool, comprising: (i) providing beads comprising 5′linked RNA primers comprising a consensus sequence; (ii) hybridizing the 5′-linked RNA primers with DNA oligonucleotides comprising a unique template sequence and a sequence complementary to the consensus sequence, wherein the DNA oligonucleotides are provided in solution; (iii) extending the hybridized RNA primers along the single-stranded template DNAs using an RNA polymerase and ribonucleoside triphosphates to obtain double-stranded DNA-RNA hybrids; and (iv) contacting the DNA-RNA hybrids with a DNase to remove the template DNAs from the DNA-RNA hybrids to obtain an RNA bead pool. 